Professional Documents
Culture Documents
Ebook Litts Drug Eruption Reaction Manual 28Th Edition Neil H Shear Online PDF All Chapter
Ebook Litts Drug Eruption Reaction Manual 28Th Edition Neil H Shear Online PDF All Chapter
Ebook Litts Drug Eruption Reaction Manual 28Th Edition Neil H Shear Online PDF All Chapter
https://ebookmeta.com/product/litt-s-drug-eruption-reaction-
manual-29th-edition-neil-h-shear/
https://ebookmeta.com/product/litt-s-drug-eruption-reaction-
manual-30th-edition-2024-neil-h-shear/
https://ebookmeta.com/product/solutions-manual-for-essentials-of-
chemical-reaction-engineering-second-edition-h-scott-fogler/
https://ebookmeta.com/product/complicated-grief-treatment-
instruction-manual-1st-edition-m-katherine-shear/
Elements of Chemical Reaction Engineering, Global
Edition, 6th Edition H. Fogler
https://ebookmeta.com/product/elements-of-chemical-reaction-
engineering-global-edition-6th-edition-h-fogler/
https://ebookmeta.com/product/vaccine-safety-manual-2nd-edition-
neil-z-miller/
https://ebookmeta.com/product/illustrated-manual-of-injectable-
fillers-neil-s-sadick/
https://ebookmeta.com/product/euro-par-2022-parallel-
processing-28th-international-conference-on-parallel-and-
distributed-computing-glasgow-uk-august-22-26-2022-proceedings-
jose-cano/
https://ebookmeta.com/product/case-reviews-in-
ophthalmology-3e-aug-26-2022-_-0323794092-_-elsevier-3rd-edition-
neil-j-friedman-peter-k-kaiser/
28th
EDITION
The right of Neil H. Shear to be identified as Editor of this work has been asserted in accordance with sections 77 and 78 of the
Copyright, Designs and Patents Act 1988.
This book contains information obtained from authentic and highly regarded sources. While all reasonable efforts have
been made to publish reliable data and information, neither the author[s] nor the publisher can accept any legal
responsibility or liability for any errors or omissions that may be made. The publishers wish to make clear that any views
or opinions expressed in this book by individual editors, authors or contributors are personal to them and do not
necessarily reflect the views/opinions of the publishers. The information or guidance contained in this book is intended
for use by medical, scientific or health-care professionals and is provided strictly as a supplement to the medical or other
professional’s own judgement, their knowledge of the patient’s medical history, relevant manufacturer’s instructions and
the appropriate best practice guidelines. Because of the rapid advances in medical science, any information or advice on
dosages, procedures or diagnoses should be independently verified. The reader is strongly urged to consult the relevant
national drug formulary and the drug companies’ and device or material manufacturers’ printed instructions, and their
websites, before administering or utilizing any of the drugs, devices or materials mentioned in this book. This book does
not indicate whether a particular treatment is appropriate or suitable for a particular individual. Ultimately it is the sole
responsibility of the medical professional to make his or her own professional judgements, so as to advise and treat patients
appropriately. The authors and publishers have also attempted to trace the copyright holders of all material reproduced in
this publication and apologize to copyright holders if permission to publish in this form has not been obtained. If any
copyright material has not been acknowledged please write and let us know so we may rectify in any future reprint.
All rights reserved. No part of this book may be reprinted or reproduced or utilised in any form or by any electronic, mechanical,
or other means, now known or hereafter invented, including photocopying and recording, or in any information storage or
retrieval system, without permission in writing from the publishers.
For permission to photocopy or use material electronically from this work, access www.copyright.com or contact the Copyright
Clearance Center, Inc. (CCC), 222 Rosewood Drive, Danvers, MA 01923, 978-750-8400. For works that are not available on
CCC please contact mpkbookspermissions@tandf.co.uk
Trademark notice: Product or corporate names may be trademarks or registered trademarks and are used only for identification
and explanation without intent to infringe.
DOI: 10.1201/9781003261803
Publisher's note: This book has been prepared from camera-ready copy provided by the authors.
Color profile: Generic CMYK printer profile
Composite Default screen
CONTENTS
Introductory notes v
Drug profiles: generic names A–Z 1
Descriptions of important reactions 375
Drugs that cause important reactions 381
Investigational drugs for the treatment of COVID-19 415
Main classes of drugs 417
Class reactions 423
ACE inhibitors 423
Antiarrhythmics 425
Antibiotics, imidazole 427
Antibiotics, macrolide 428
Anticonvulsants 429
Antidepressants, tricyclic 432
Antihistamines (H1) 433
Antimalarials 434
Antipsychotics 436
Antiretrovirals 438
Benzodiazepines 440
Beta blockers 441
Biologics, immune checkpoint inhibitors 442
Biologics, monoclonal antibodies 444
Bisphosphonates 448
Calcium channel blockers 449
Cephalosporins 451
Corticosteroids, topical 452
Disease-modifying antirheumatic drugs (DMARDS) 454
DPP-4 inhibitors 459
Epidermal growth factor receptor (EGFR) inhibitors 460
Fluoroquinolones 463
Non-steroidal anti-inflammatory drugs (NSAIDS) 465
Proton pump inhibitors (PPI) 468
Statins 470
TNF inhibitors 471
Tyrosine-kinase inhibitors 474
Genetic tables 478
Concordance of synonyms and trade names with
generic names 491
iii
A note on ADRs
The incidence and severity of ADRs are influenced by a number of factors:
1. Patient-related factors:
Age – geriatric, pediatric, adolescent . . . older patients are taking more medications-hence more of a possibility of develop-
ing reactions; pediatric patients have more delicate skins; hormonal changes occur in adolescents . . . All these factors play
roles in the development of possible adverse reactions.
Gender – male or female – and if the latter, then pregnant/breast-feeding/menopausal . . .
Disease – not only the disease being treated, but also other pre-existing health conditions and comorbid diseases. For
example, atopic patients are at increased risk for serious allergic reactions; also, there would be an increased risk for hyper-
sensitivity drug reactions if the patient has asthma or lupus erythematosus.
Genetics – a patient could have abnormal drug metabolism by cytochrome P450 due to inheriting abnormal alleles.
Geography – patients living in sunny climes could develop photoxicities from photosensitizing drugs more readily than
those who inhabit cooler, less sunny climates.
2. Drug-related factors:
Type/class of drug – for example, there is a heightened risk of angioedema with the use of ACE inhibitors (see further the
tables of class reactions).
Duration of therapy – the longer a patient maintains the therapy, the greater the possibility that he/she could develop a
reaction.
Dosage – the greater the dosage, the more likely an adverse side effect.
Bioavailability – the extent to and rate at which the drug enters systemic circulation, thereby accessing the site of action.
Interactions with other drugs – for example, synergistic QT prolongation can occur when two QT prolonging agents, such
as erythromycin + ritonavir, are used together.
Route of administration – intramuscular, intravenous, subcutaneous, and topical administrations are more likely to cause
hypersensitivity reactions; oral medications are less likely to result in drug hypersensitivity.
The terms “drug allergy,” “drug hypersensitivity,“ and “drug reaction” are often used interchangeably. “Drug allergy” specifi-
cally refers to a reaction mediated by IgE; “drug hypersensitivity” is an immune-mediated response to a drug agent in a sensi-
tized patient; and “drug reactions” comprise all adverse events related to drug administration, regardless of etiology.
vi
vii
viii
I’ll start off with a real referral sent to me a few years ago (I expect it will sound familiar to all dermatologists):
“Dear Neil,
I am just seeing a patient at the hospital.
The patient took amoxicillin and clarithromycin 1 week before & ceftriaxone 45 min before getting a rash.
I think it very unlikely that ceftriaxone is the cause. As far as I know he never had it before.
The reason for this note is that our Respiratory Physician feels strongly that ceftriaxone is the cause.
What do you think?”
What I do like about this is the fact that this is a written (email) request, so any reply I give has some demonstrable existence,
as against a phone call or hall chat relying on memory only.
However, a common mistake would be to answer the question “What do you think?” There is very limited information about
this patient whom I did not see and will never see. The first step in a proper consultation is DIAGNOSIS of the possible drug
reaction. There are 3 key components for making a diagnosis:
– Appearance of the rash
– Systemic issues
– Histology
My mnemonic is Remember: Appearance, Systemic, Histology (RASH).
Thinking back on the referral sent to me I have very little information to help make a diagnosis.
What was the “rash” and were there systemic symptoms and signs? I don’t know. So I will need to ask for more detailed infor-
mation if this consultation continues.
The second step is to determine CAUSALITY. Note the referral is focused on an assumption that I will pick a single drug that
caused the “rash”. Unfortunately, that is not how life works. There are at a minimum 3 possible causes that we know of from
the history of drugs given. We don’t know if the patient was on other drugs or has a drug allergy history. In this case I will have
to assume there are NO systemic features and that the “rash” is a “simple exanthem”.
Causality assessments demand:
– A quantitative approach (numbers matter)
– Using a Bayesian type of approach we can generate probabilities that each drug we know of might have caused a reaction.
So now I need to see what the baseline rate of “rash” is for each drug. This is where Litt comes in . . .
Amoxicillin
Looking at the Amoxicillin listing in the database (Fig 1) or the Amoxicillin summary in the manual I can see that there are 33
reports of the reaction and that the background rate is estimated at >5%. This is not the final step, but it gives me some
evidence to demonstrate that, although each of these drugs
could cause rash, one is much more likely than the others.
Figure 1
ix
After we have the background rate from Litt we can think of data that might modify the background rate. Nothing is as helpful
as knowing the timing of drug exposure to onset of a rash. In this instance we know that aminopenicillin rashes come on
around day 8 to 10 after exposure. That is very powerful additional information.
Ceftriaxone
There are comparatively few (7) reports and lower reported background rates (none in the package insert information) for
this reaction in the database (Fig 2) and manual for a drug that is widely used. Clearly exanthems are not a major clinical issue,
and the figures here are reassuringly low – not nearly as high as Amoxicillin, although not impossible.
Figure 2
Clarithromycin
Figure 3 shows the very few (3) reports from the database and manual of this drug causing a rash; the lack of any reported
background rate supports the conclusion it is not a major clinical issue.
Figure 3
We have to come to some conclusion and all possibilities need to be represented. Based on Amoxicillin being a common cause
of an exanthem (AND on the timing), we have to give it a big lead. Then we think of “I don’t know” and “I will never know”,
which I always mark down as 15% each. We now know the other antibiotics have a much small risk. So 30% for the
unknowns, 5% or so for the drugs that were unlikely, leaves the remainder for Amoxicillin.
The numbers are approximations based on the data to hand. Having other unknowns reflects real life: maybe it was due to
some contrast media? Or a comorbid risk? Or dozens of other possibilities. And truly sometimes we never know.
Now I am ready (and armed with data I can defend rationally) to send my report back to the referring doctor:
“Dear colleague
Thank you for sending information about your patient. I have not seen the patient and some key information is missing. My report is
based on what information I have but clearly that could change with more data.
Assuming the patient had a simple exanthem and no fever etc., the estimated likelihood of what caused the rash is as follows:
Amoxicillin: 65%
Ceftriaxone: 4%
Clarithromycin: 1%
Other unknown exposures or risks: 15%
We will never know: 15%”
CONCLUSIONS
LESSON 1: Look for good quality clinical data.
LESSON 2: Give opinions in text, not conversation.
LESSON 3: Use a structured summary that is uniform, every time, to increase the impact and be on target.
LESSON 4: Be quantitative; it is clear and respected.
I hope this enhances your search for quality information and enhanced patient safety.
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 1
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Local Local
Infusion-related reactions [4] Injection-site reaction (4%) ABIRATERONE
Infusion-site reactions (9%) [5] Neuromuscular/Skeletal Trade name: Zytiga (Janssen Biotech)
Injection-site erythema [3] Back pain (17%) Indications: Metastatic castration-resistant
Injection-site hematoma [2] Other prostate cancer (in combination with prednisone)
Injection-site pain [3] Death [3] Class: CYP17 inhibitor, Enzyme inhibitor
Injection-site pruritus [2] Half-life: 12 hours
Injection-site reaction (3%) [8] Clinically important, potentially hazardous
Neuromuscular/Skeletal ABEMACICLIB interactions with: atazanavir, carbamazepine,
Asthenia / fatigue [2] clarithromycin, CYP3A4 inducers or inhibitors,
Back pain (7%) [2] Trade name: Verzenio (Lilly)
indinavir, itraconazole, ketoconazole, nefazodone,
Pain in extremities (3%) Indications: Hormone receptor-positive, human
nelfinavir, phenobarbital, phenytoin, rifabutin,
Respiratory epidermal growth factor 2-negative advanced or
metastatic breast cancer, either as monotherapy rifampin, rifapentine, ritonavir, saquinavir,
Bronchitis (<13%) [4] telithromycin, thioridazine, voriconazole
or in combination with fulvestrant, or as inital
Cough (5–8%) Pregnancy category: X
endocrine-based therapy with an aromatase
Influenza (5–13%) [2] Important contra-indications noted in the
inhibitor
Nasopharyngitis (12%) [6] prescribing guidelines for: nursing mothers;
Pharyngitis [3] Class: CDK4/6 inhibitor
Half-life: 18 hours pediatric patients
Pneumonia (<5%) [7] Note: Contra-indicated in women who are or
Pulmonary toxicity [2] Clinically important, potentially hazardous
interactions with: grapefruit juice, may become pregnant.
Rhinitis (<5%) [2]
Sinusitis (5–13%) [3] ketoconazole, strong CYP3A4 inducers or
inhibitors Skin
Tuberculosis [2] Edema (27%) [21]
Upper respiratory tract infection (>10%) Pregnancy category: N/A (Can cause fetal
harm) Hot flashes (19%) [4]
[9]
Important contra-indications noted in the Cardiovascular
Other prescribing guidelines for: nursing mothers; Arrhythmias (7%)
Adverse effects [24] pediatric patients Atrial fibrillation [3]
Death [2] Cardiac failure (2%)
Infection (36–54%) [25] Cardiotoxicity [6]
Hair
Alopecia (12%) Chest pain (4%)
ABCIXIMAB Hypertension (9%) [27]
Mucosal
Tachycardia [3]
Stomatitis (oral mucositis) (14%)
Synonym: C7E3 Xerostomia (dry mouth) (17%) Central Nervous System
Trade name: ReoPro (Janssen Biotech) Headache [2]
Indications: Thrombotic arterial disease Central Nervous System
Anorexia [3] Endocrine/Metabolic
Class: Antiplatelet, Glycoprotein IIb/IIIa inhibitor, ALT increased (11%) [8]
Monoclonal antibody Dysgeusia (taste perversion) (12%)
Fever (pyrexia) (11%) AST increased (31%) [4]
Half-life: 10–30 minutes – given intravenously Hypercholesterolemia [2]
Clinically important, potentially hazardous
Headache (20%)
Vertigo / dizziness (11%) Hyperglycemia [2]
interactions with: anticoagulants, antiplatelets, Hypertriglyceridemia (63%)
collagenase, dasatinib, dextran, drotrecogin alfa, Endocrine/Metabolic
Hypokalemia [27]
fondaparinux, glucosamine, herbals with ALT increased (31%)
Appetite decreased (45%) [3] Gastrointestinal/Hepatic
anticoagulant properties, lepirudin, monoclonal Constipation [8]
antibodies, NSAIDs, omega-3 fatty acids, AST increased (30%)
Dehydration (10%) Diarrhea (18%) [6]
pentosan, pentoxifylline, prostacyclin analogues, Dyspepsia / functional dyspepsia /
reteplase, salicylates, thrombolytic agents, Serum creatinine increased (13%) [3]
Weight loss (14%) [2] gastroparesis (6%)
tositumomab & iodine131, trastuzumab Hepatic (liver) disorder / hepatic (liver)
Pregnancy category: C Gastrointestinal/Hepatic
dysfunction [2]
Important contra-indications noted in the Abdominal pain (39%) [2]
Hepatotoxicity / liver injury / acute liver
prescribing guidelines for: nursing mothers; Constipation (17%)
injury / drug-induced liver injury (DILI)
pediatric patients Diarrhea (90%) [11]
(2%) [13]
Nausea (64%) [9]
Nausea [9]
Vomiting (35%) [4]
Skin Vomiting [2]
Anaphylactoid reactions / anaphylaxis Hematologic
Genitourinary
(includes anaphylactic shock) [3] Anemia (25%) [3]
Nocturia (6%)
Peripheral edema (2%) Leukocytopenia (leukopenia) (17%) [5]
Urinary frequency (7%)
Neutropenia (neutrophils decreased) (37%)
Cardiovascular Urinary tract infection (12%) [3]
[9]
Bradycardia / sinus bradycardia (5%) Hematologic
Thrombocytopenia (20%) [3]
Chest pain (9%) Anemia [6]
Hypotension (15%) Neuromuscular/Skeletal
Febrile neutropenia [2]
Myocardial infarction [4] Arthralgia (15%)
Neutropenia (neutrophils decreased) [2]
Asthenia / fatigue (65%) [9]
Central Nervous System Thrombocytopenia [3]
Headache (6%) Respiratory
Neuromuscular/Skeletal
Pain (5%) Cough (19%)
Arthralgia [6]
Gastrointestinal/Hepatic Other Asthenia / fatigue [14]
Nausea (12%) Infection (31%) Back pain [6]
Vomiting (7%) Bone or joint pain (30%) [9]
Hematologic Myalgia/Myopathy (26%)
Bleeding [2] Pain in extremities [3]
Thrombocytopenia [15] Rhabdomyolysis [3]
2 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Respiratory Other
Cough (11%) ACAMPROSATE Adverse effects [3]
Dyspnea / shortness of breath [3] Trade name: Campral (Forest) (Lipha) Infection (<10%)
Nasopharyngitis [2] Indications: Alcohol dependence
Upper respiratory tract infection (5%) [2]
Other
Class: Amino acid (synthetic)
Half-life: 20–33 hours
ACARBOSE
Adverse effects [8] Clinically important, potentially hazardous Trade names: Glucobay (Bayer), Precose
interactions with: none known (Bayer)
Pregnancy category: C Indications: Non-insulin dependent diabetes
ACALABRUTINIB Important contra-indications noted in the Type II
Trade name: Calquence (AstraZeneca) prescribing guidelines for: nursing mothers; Class: Alpha-glucosidase inhibitor, Antidiabetic
Indications: Treatment of adult patients with pediatric patients Half-life: 2 hours
mantle cell lymphoma (MCL) who have received Note: Contra-indicated in patients with severe Clinically important, potentially hazardous
at least one prior therapy renal impairment. interactions with: alcohol, anabolic steroids,
Class: Bruton’s tyrosine kinase (BTK) inhibitor beta blockers, cholestyramine, corticosteroids,
Half-life: <3 hours Skin diazoxide, digoxin, diuretics, estrogens,
Clinically important, potentially hazardous Diaphoresis (2%) hypoglycemic agents, MAO inhibitors, neomycin,
interactions with: antacids, famotidine, H2- Peripheral edema (<10%) orlistat, pancreatin, pegvisomant, pramlintide,
receptor antagonists, itraconazole, proton pump Pruritus (itching) (4%) [2] progestogens, somatropin, testosterone
inhibitors, ranitidine, rifampin, strong CYP3A Mucosal Pregnancy category: B
inducers, strong or moderate CYP3A inhibitors Xerostomia (dry mouth) (2%) Important contra-indications noted in the
Pregnancy category: N/A (May cause fetal Cardiovascular prescribing guidelines for: nursing mothers;
toxicity based on findings in animal studies) Chest pain (<10%) pediatric patients
Important contra-indications noted in the Hypertension (<10%) Note: Contra-indicated in patients with diabetic
prescribing guidelines for: nursing mothers; Palpitation (<10%) ketoacidosis or cirrhosis; also in patients with
pediatric patients Vasodilation (1–10%) inflammatory bowel disease, colonic ulceration,
partial intestinal obstruction or in patients
Central Nervous System predisposed to intestinal obstruction.
Skin Amnesia (<10%)
Bruise / bruising / contusion / ecchymosis Anorexia (2–5%)
(ecchymoses) (21%) [2] Anxiety (5–8%) [2] Skin
Hematoma (8%) Chills (<10%) AGEP [2]
Malignancies (11%) Depression (4–8%) Gastrointestinal/Hepatic
Petechiae (21%) Headache (<10%) [2] Abdominal distension [2]
Rash (18%) Insomnia (6–9%) Abdominal pain (19%)
Mucosal Pain (2–4%) Diarrhea (31%)
Epistaxis (nosebleed) (6%) Paresthesias (2–3%) Flatulence (74%) [3]
Cardiovascular Somnolence (drowsiness) (<10%) Hepatitis [2]
Atrial fibrillation (3%) Suicidal ideation (1–10%) Hepatotoxicity / liver injury / acute liver
Atrial flutter (3%) Syncope / fainting (<10%) injury / drug-induced liver injury (DILI) [3]
Hypertension [2] Tremor (<10%) Pneumatosis intestinalis / pneumatosis
Vertigo / dizziness (3–4%) cystoides intestinalis [8]
Central Nervous System
Fever (pyrexia) [2] Endocrine/Metabolic Other
Headache (39%) [7] Appetite increased (<10%) Adverse effects [5]
Endocrine/Metabolic Libido decreased (<10%)
Weight gain (<10%)
Weight gain [4]
Gastrointestinal/Hepatic
ACEBUTOLOL
Gastrointestinal/Hepatic
Abdominal pain (15%) Abdominal pain (<10%) Trade name: Sectral (Sanofi-Aventis)
Constipation (15%) Constipation (<10%) Indications: Hypertension, angina, ventricular
Diarrhea (31%) [6] Diarrhea (16%) [6] arrhythmias
Nausea (19%) [2] Dyspepsia / functional dyspepsia / Class: Antiarrhythmic class II, Beta adrenergic
Vomiting (13%) gastroparesis (<10%) blocker, Beta blocker
Flatulence (<4%) [2] Half-life: 3–7 hours
Hematologic Nausea (3–4%) [2] Clinically important, potentially hazardous
Anemia (46%) Vomiting (<10%) [2]
Hemorrhage (8%) interactions with: ACE inhibitors, adrenergic
Neutropenia (neutrophils decreased) (36%) Genitourinary neurone blockers, alcohol, aldesleukin, alpha
Thrombocytopenia (44%) Impotence (<10%) blockers, alprostadil, amiodarone, angiotensin II
Neuromuscular/Skeletal receptor antagonists, antiarrhythmics,
Neuromuscular/Skeletal antidiabetics, anxiolytics and hypnotics, baclofen,
Arthralgia [2] Arthralgia (<10%)
Asthenia / fatigue (5–7%) calcium channel blockers, cardiac glycosides,
Asthenia / fatigue (28%) [3]
Myalgia/Myopathy (21%) [2] Back pain (<10%) clonidine, corticosteroids, diazoxide, diltiazem,
Myalgia/Myopathy (<10%) disopyramide, diuretics, ergotamine, estrogens,
Respiratory flecainide, general anesthetics, hydralazine,
Pneumonia [3] Ocular
Abnormal vision (<10%) insulin, levodopa, MAO inhibitors, mefloquine,
Upper respiratory tract infection [2] methyldopa, methysergide, minoxidil, moxisylyte,
Respiratory
Bronchitis (<10%) moxonidine, nifedipine, nitrates, nitroprusside,
Cough (<10%) NSAIDs, phenothiazines, pilocarpine, prazosin,
Dyspnea / shortness of breath (<10%) tizanidine, verapamil
Flu-like syndrome (<10%) Pregnancy category: B
Pharyngitis (<10%)
Rhinitis (<10%)
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 3
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
4 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Pruritus (itching) [5] Anaphylactoid reactions / anaphylaxis Important contra-indications noted in the
Purpura [6] (includes anaphylactic shock) [3] prescribing guidelines for: pediatric patients
Rash [IV] [3] Exanthems [2]
Stevens-Johnson syndrome [11] Pemphigus [2] Cardiovascular
Toxic epidermal necrolysis [14] Stevens-Johnson syndrome [7] Bradycardia / sinus bradycardia [7]
Urticaria / hives [17] Toxic epidermal necrolysis [2] Hypotension [8]
Vasculitis (angiitis) / cutaneous vasculitis Central Nervous System Ocular
(angiitis) [4] Depression [2] Intraocular pressure increased [5]
Mucosal Dysgeusia (taste perversion) (>10%) [8]
Respiratory
Xerostomia (dry mouth) [3] Paresthesias [6] Bronchospasm [2]
Cardiovascular Endocrine/Metabolic
Hypertension [IV] [3] Acidosis (including lactic acidosis) [3]
Hypotension [2] Libido decreased [2] ACETYLCYSTEINE
Central Nervous System Weight loss [2]
Agitation [IV] (>5%) Gastrointestinal/Hepatic Synonyms: N-acetylcysteine; L-Cysteine; NAC
Fever (pyrexia) [IV] (5%) Diarrhea [2] Indications: Emphysema, bronchitis,
Headache [IV] (10%) [5] Dyspepsia / functional dyspepsia / tuberculosis, bronchiectasis, tracheostomy care,
Insomnia [IV] (7%) gastroparesis [2] antidote for acetaminophen toxicity
Somnolence (drowsiness) [8] Nausea [2] Class: Antidote, Antioxidant
Vertigo / dizziness [15] Vomiting [2] Half-life: N/A
Clinically important, potentially hazardous
Endocrine/Metabolic Neuromuscular/Skeletal interactions with: carbamazepine, nitroglycerin
Acidosis (including lactic acidosis) [3] Asthenia / fatigue [4] Pregnancy category: B
Gastrointestinal/Hepatic Ocular Note: As an antidote, it is difficult to differentiate
Abdominal distension [2] Choroidal detachment [2] side effects due to the drug from those due to the
Abdominal pain [IV] [3] Corneal edema [2] effects of the poison.
Constipation [IV] (>5%) [7] Glaucoma [5]
Diarrhea [IV] [2] Myopia [2] Skin
Hepatotoxicity / liver injury / acute liver Renal Anaphylactoid reactions / anaphylaxis
injury / drug-induced liver injury (DILI) [70] Nephrolithiasis [3] (includes anaphylactic shock) (8–18%) [14]
Nausea [IV] (34%) [18]
Angioedema [6]
Pancreatitis / acute pancreatitis [6] Flushing / rubefaction (<8%) [2]
Vomiting (15%) [16] ACETOHEXAMIDE Pruritus (itching) (<4%) [3]
Hematologic Rash (2–4%) [4]
Trade name: Dymelor (Barr)
Thrombocytopenia [2] Urticaria / hives (6–8%)
Indications: Non-insulin dependent diabetes
Neuromuscular/Skeletal Type ll Cardiovascular
Rhabdomyolysis [4] Class: Sulfonylurea Tachycardia (<4%)
Renal Half-life: 1–6 hours Central Nervous System
Nephrotoxicity / kidney injury / acute kidney Clinically important, potentially hazardous Seizures [2]
injury (AKI) / drug-induced kidney injury [9] interactions with: phenylbutazones Gastrointestinal/Hepatic
Renal failure [3] Pregnancy category: C Diarrhea [2]
Respiratory Important contra-indications noted in the Nausea (<6%) [3]
Asthma [3] prescribing guidelines for: nursing mothers Vomiting (2–10%) [2]
Pulmonary toxicity [IV] (>5%) Note: Acetohexamide is a sulfonamide and can
Other
Other be absorbed systemically. Sulfonamides can
Adverse effects [2]
Adverse effects [16] produce severe, possibly fatal, reactions such as
Death [2]
Death [6] toxic epidermal necrolysis and Stevens-Johnson
syndrome.
ACIPIMOX
ACETAZOLAMIDE Skin
Photosensitivity (<10%) Trade name: Olbetam (Pharmacia)
Trade name: Diamox (Duramed) Rash (<10%) Indications: Hyperlipoproteinemia
Indications: Epilepsy, glaucoma Urticaria / hives (<10%) Class: Cholesterol antagonist
Class: Carbonic anhydrase inhibitor, Diuretic Half-life: 2 hours
Half-life: 2–6 hours Endocrine/Metabolic
Hypoglycemia [2] Clinically important, potentially hazardous
Clinically important, potentially hazardous interactions with: fibrates, statins
interactions with: arsenic, aspirin, ephedra, Pregnancy category: N/A (Not recommended
indacaterol, lisdexamfetamine, lithium,
metformin, mivacurium, triamcinolone
ACETYLCHOLINE in pregnancy)
Important contra-indications noted in the
Pregnancy category: C Trade name: Miochol (Novartis) prescribing guidelines for: nursing mothers
Important contra-indications noted in the Indications: Cataract surgery, in penetrating
prescribing guidelines for: the elderly; nursing keratoplasty, iridectomy and other anterior Skin
mothers; pediatric patients segment surgery where rapid miosis may be Flushing / rubefaction [9]
Note: Acetazolamide is a sulfonamide and can be required
absorbed systemically. Sulfonamides can produce Class: Ophthalmic agent, miotic,
severe, possibly fatal, reactions such as toxic Parasympathomimetic
epidermal necrolysis and Stevens-Johnson Half-life: N/A
syndrome. Clinically important, potentially hazardous
interactions with: none known
Skin Pregnancy category: C
AGEP [2]
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 5
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
6 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 7
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
8 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 9
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
10 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 11
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
12 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 13
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
14 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
surgery and death) prompted alosetron’s grapefruit juice, indinavir, itraconazole, Cardiovascular
voluntary withdrawal from the US market in ivermectin, kava, ketoconazole, posaconazole, Bradycardia / sinus bradycardia (<10%)
November 2000. Public request prompted its propoxyphene, ritonavir, saquinavir, St John’s Hypertension (<10%)
reintroduction in 2002 under a Risk Management wort, telaprevir, tipranavir Hypotension (<10%)
Plan, including a more restricted indication and a Pregnancy category: D Tachycardia (<10%)
Prescribing Program for Lotronex. Only licensed Important contra-indications noted in the Central Nervous System
for use in female patients. Contra-indicated in prescribing guidelines for: the elderly; nursing Fever (pyrexia) (>10%)
patients with constipation or a history of chronic mothers; pediatric patients Headache (>10%)
or severe constipation or sequelae from Pain (>10%)
constipation; intestinal obstruction, stricture, Skin Vertigo / dizziness (>10%)
toxic megacolon, gastrointestinal perforation, Dermatitis (4%) [5] Gastrointestinal/Hepatic
and/or adhesions; ischemic colitis; impaired Diaphoresis (16%) Diarrhea (<10%)
intestinal circulation, thrombophlebitis, or Edema (5%)
hypercoagulable state; Crohn’s disease or Genitourinary
Photosensitivity [4] Erectile dysfunction (prolonged erection /
ulcerative colitis; diverticulitis; severe hepatic Pruritus (itching) (<10%) [2]
impairment. >4 hours) (4%)
Rash (11%) [4] Penile pain (>10%)
Warning: SERIOUS GASTROINTESTINAL
ADVERSE REACTIONS Mucosal Priapism (4%) [8]
Sialopenia (33%) Urethral burning (>10%) [2]
Sialorrhea (ptyalism; hypersalivation) (4%) Local
Gastrointestinal/Hepatic Xerostomia (dry mouth) (15%) [6]
Abdominal distension (2%) Application-site burning [3]
Abdominal pain (<7%) [3] Cardiovascular Application-site erythema [3]
Colitis [12] Hypotension (<10%) Application-site pain [2]
Constipation (9–29%) [14] Central Nervous System Application-site pruritus [2]
Diarrhea (2–3%) Cognitive impairment (>10%) Injection-site ecchymoses (<10%)
Flatulence (<3%) Coma [2] Injection-site hematoma (3%)
Gastroenteritis (>3%) Depression (>10%) Injection-site pain (2%)
Gastroesophageal reflux (2%) Dysarthria (>10%) Neuromuscular/Skeletal
Hemorrhoids (<3%) Incoordination (<10%) Back pain (<10%)
Nausea (6%) Memory loss/memory impaired [2] Respiratory
Vomiting (<3%) Neurotoxicity [2] Apnea (>10%)
Genitourinary Paresthesias (2%) Cough (<10%)
Urinary tract infection (>3%) Restlessness [2] Flu-like syndrome (<10%)
Sedation [2] Sinusitis (<10%)
Neuromuscular/Skeletal Seizures (<10%) [2]
Asthenia / fatigue (3%) Somnolence (drowsiness) (>10%)
Muscle spasm (3%) ALTEPLASE
Endocrine/Metabolic
Respiratory Galactorrhea [2]
Cough (>3%) Synonym: tPA
Nasopharyngitis (>3%) Genitourinary Trade name: Activase (Genentech)
Sinusitis (>3%) Micturition difficulty (>10%) Indications: Acute myocardial infarction, acute
Upper respiratory tract infection (>3%) Neuromuscular/Skeletal pulmonary embolism
Other Asthenia / fatigue (>10%) [2] Class: Fibrinolytic, Plasminogen activator
Adverse effects [5] Half-life: 30–45 minutes
Clinically important, potentially hazardous
ALPROSTADIL interactions with: defibrotide, nitroglycerin,
ALPHA-LIPOIC ACID Synonyms: PGE; prostaglandin E1 ticlopidine
Trade names: Caverject (Pfizer), Edex Pregnancy category: C
Synonym: ALA Important contra-indications noted in the
(Schwarz), Muse (Vivus), Prostin VR (Pfizer)
Indications: Diabetic neuropathy, vasodilation, prescribing guidelines for: the elderly; nursing
Indications: Impotence, to maintain patent
photoaging mothers
ductus arteriosus
Class: Dietary supplement
Class: Prostaglandin
Half-life: N/A
Half-life: 5–10 minutes Skin
Clinically important, potentially hazardous
Clinically important, potentially hazardous Anaphylactoid reactions / anaphylaxis
interactions with: none known
interactions with: acebutolol, alfuzosin, (includes anaphylactic shock) [5]
captopril, cilazapril, enalapril, fosinopril, Angioedema [12]
Skin irbesartan, lisinopril, olmesartan, quinapril, Bruise / bruising / contusion / ecchymosis
Rash [2] ramipril (ecchymoses) (<10%)
Central Nervous System Pregnancy category: D (not indicated for use in Purpura (<10%)
Vertigo / dizziness [2] women) Central Nervous System
Important contra-indications noted in the Fever (pyrexia) (<10%)
prescribing guidelines for: pediatric patients Intracranial hemorrhage [8]
ALPRAZOLAM Warning: APNEA (in neonates with congenital Gastrointestinal/Hepatic
Trade name: Xanax (Pfizer) heart defects) Hemorrhagic colitis (5%)
Indications: Anxiety, depression, panic attacks Hematologic
Class: Benzodiazepine Skin Bleeding [3]
Half-life: 11–16 hours Edema (<10%) Hemorrhage (4%)
Clinically important, potentially hazardous Flushing / rubefaction (>10%) Other
interactions with: alcohol, amprenavir, Penile rash (<10%) Death [4]
aprepitant, boceprevir, clarithromycin, CNS Mucosal
depressants, darunavir, delavirdine, digoxin, Nasal congestion (<10%)
efavirenz, fluconazole, fluoxetine, fluvoxamine,
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 15
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
16 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Dermatitis [3]
Flushing / rubefaction (>10%) [4] AMILORIDE AMINO-GLUTETHIMIDE
Rash [6] Trade names: Midamor (Merck), Moduretic Trade name: Cytadren (Novartis)
Stevens-Johnson syndrome [3] (Merck) Indications: Suppression of adrenal function,
Toxic epidermal necrolysis [3] Indications: Prevention of hypokalemia metastatic carcinoma
Mucosal associated with kaliuretic diuretics, management Class: Aromatase inhibitor
Mucositis [4] of edema in hypertension Half-life: 7–15 hours
Xerostomia (dry mouth) [7] Class: Diuretic, potassium-sparing Clinically important, potentially hazardous
Cardiovascular Half-life: 6–9 hours interactions with: betamethasone,
Hypotension (15–61%) [5] Clinically important, potentially hazardous dexamethasone, doxercalciferol, oxtriphylline,
Central Nervous System interactions with: ACE inhibitors, benazepril, triamcinolone
Chills (>10%) captopril, cyclosporine, enalapril, fosinopril, Pregnancy category: D
Dysgeusia (taste perversion) [2] lisinopril, magnesium, metformin, moexipril, Important contra-indications noted in the
Fever (pyrexia) [3] potassium salts, quinapril, quinidine, ramipril, prescribing guidelines for: the elderly; nursing
Endocrine/Metabolic spironolactone, trandolapril, zofenopril mothers; pediatric patients
Hypocalcemia [2] Pregnancy category: B
Note: Moduretic is amiloride and Skin
Gastrointestinal/Hepatic
hydrochlorothiazide. Hydrochlorothiazide is a Exanthems [8]
Nausea (53–96%) [2]
sulfonamide and can be absorbed systemically. Lupus erythematosus (>10%)
Vomiting (53–96%) [2]
Sulfonamides can produce severe, possibly fatal, Pruritus (itching) (5%)
Respiratory reactions such as toxic epidermal necrolysis and Rash (>10%)
Dyspnea / shortness of breath (4%) Stevens-Johnson syndrome. Hair
Other Hirsutism (<10%)
Allergic reactions [2] Skin Mucosal
Photosensitivity [4] Oral mucosal eruption [2]
AMIKACIN Central Nervous System Neuromuscular/Skeletal
Headache (<10%) Myalgia/Myopathy (3%)
Trade name: Amikacin sulfate (Bedford) Vertigo / dizziness (<10%)
Indications: Short-term treatment of serious Endocrine/Metabolic
infections due to gram-negative bacteria Gynecomastia (<10%) AMINOLEVULINIC ACID
Class: Antibiotic, Antibiotic; aminoglycoside, Hyperkalemia [2]
Drug-resistant antituberculosis agent Trade names: Ameluz (Biofrontera), Levulan
Genitourinary
Half-life: 1.5–2.5 hours (adults) Kerastick (Dusa)
Impotence (<10%)
Clinically important, potentially hazardous Indications: Non-hyperkeratotic actinic
interactions with: adefovir, aldesleukin,
Neuromuscular/Skeletal keratoses of face and scalp
Asthenia / fatigue (<10%) Class: Photosensitizer, Protoporphyrin IX (PpIX)
aminoglycosides, atracurium, bumetanide,
Myalgia/Myopathy (<10%) (wakefulness promoting agent)
cephalexin, doxacurium, ethacrynic acid,
furosemide, succinylcholine, teicoplanin, Respiratory Half-life: 20–40 hours
torsemide Cough (<10%) Clinically important, potentially hazardous
Pregnancy category: D Dyspnea / shortness of breath (<10%) interactions with: none known
Important contra-indications noted in the Pregnancy category: C
prescribing guidelines for: nursing mothers; Important contra-indications noted in the
pediatric patients
AMINOCAPROIC ACID prescribing guidelines for: nursing mothers;
Note: Aminoglycosides may cause neurotoxicity pediatric patients
Trade name: Amicar (Xanodyne)
and/or nephrotoxicity. Note: In photodynamic therapy: to be used in
Indications: To provide hemostasis in the
conjunction with the relevant illuminator as
treatment of fibrinolysis
approved by the manufacturer.
Skin Class: Antifibrinolytic
Dermatitis [3] Half-life: 1–2 hours
Exanthems [2] Clinically important, potentially hazardous Skin
Central Nervous System interactions with: none known Burning / skin burning sensation (>50%) [6]
Neurotoxicity (<10%) Pregnancy category: C Crusting (64–71%) [2]
Important contra-indications noted in the Dermatitis [2]
Ocular Desquamation [2]
Macular infarction [3] prescribing guidelines for: nursing mothers;
pediatric patients Edema (35%) [9]
Otic Erosions (14%) [2]
Hearing loss (hypoacusis) [6] Erythema (99%) [13]
Ototoxicity (<10%) [9] Skin
Exfoliative dermatitis (from topical
Tinnitus [3] Dermatitis [4]
treatment) [3]
Purpura [2]
Renal Hypomelanosis (22%)
Rash (<10%)
Nephrotoxicity / kidney injury / acute kidney Photosensitivity [3]
injury (AKI) / drug-induced kidney injury Neuromuscular/Skeletal Pigmentation (from topical treatment) (22%)
(<10%) [11] Myalgia/Myopathy (<10%) [7]
Rhabdomyolysis [11] Pruritus (itching) (25%) [2]
Renal Pustules (<4%)
Nephrotoxicity / kidney injury / acute kidney Scaling (64–71%)
injury (AKI) / drug-induced kidney injury [2] Stinging (>50%) [2]
Ulcerations (4%)
Vesiculation (4%) [2]
Cardiovascular
Hypotension [2]
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 17
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
18 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 19
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
20 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 21
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
22 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Hematologic
Anemia [2] ANASTROZOLE ANDROSTENEDIONE
Neuromuscular/Skeletal Trade name: Arimidex (AstraZeneca) Synonym: N/A
Arthralgia (<5%) Indications: Breast carcinoma (localized – Other common trade names: Andro,
Asthenia / fatigue (23%) advanced or metastatic) Androstene
Back pain (6%) Class: Antineoplastic, Aromatase inhibitor Indications: Enhanced athletic performance,
Leg cramps (<5%) Half-life: 50 hours increased energy, to keep red blood cells healthy
Myalgia/Myopathy (<5%) Clinically important, potentially hazardous Class: Aromatase inhibitor
Otic interactions with: estradiol, estrogens, Half-life: N/A
Tinnitus (<5%) tamoxifen Clinically important, potentially hazardous
Respiratory Pregnancy category: N/A (Contra-indicated in interactions with: none known
Dyspnea / shortness of breath (12%) women of premenopausal endocrine status, Note: Protease inhibitors cause dyslipidemia
Flu-like syndrome (<5%) including pregnant women) which includes elevated triglycerides and
Other Important contra-indications noted in the cholesterol and redistribution of body fat centrally
Adverse effects (<5%) prescribing guidelines for: nursing mothers to produce the so-called ‘protease paunch’,
Note: The efficacy of anastrozole in the breast enlargement, facial atrophy, and ‘buffalo
treatment of pubertal gynecomastia in adolescent hump’
ANAKINRA boys and in the treatment of precocious puberty In 2004 the FDA requested companies to stop
in girls with McCune-Albright syndrome has not distributing products containing androstenedione.
Trade name: Kineret (Amgen) been demonstrated. Studies have shown that it does not increase
Indications: Rheumatoid arthritis, neonatal- muscle mass and that it poses the same kind of
onset multisystem inflammatory disease Skin health risks as anabolic steroids, including
Class: Biologic, Biologic disease-modifying Flushing / rubefaction (>5%) abnormal elevations in serum estrogen, increased
antirheumatic drug (bDMARD), Covid-19 Hot flashes (12–36%) [13] risk of prostate, pancreatic and endometrial
putative drug, Disease-modifying antirheumatic Lupus erythematosus [3] cancers, and increased cardiovascular disease
drug (DMARD), Interleukin-1 receptor antagonist Peripheral edema (10%) risk.
(IL-IRa) Pruritus (itching) (2–5%)
Half-life: 4–6 hours Rash (6–11%) [2] Skin
Clinically important, potentially hazardous Vasculitis (angiitis) / cutaneous vasculitis Acneiform eruption / acneiform dermatitis /
interactions with: abatacept, adalimumab, (angiitis) [2] acneiform rash [2]
certolizumab, etanercept, golimumab, infliximab,
Hair Other
lenalidomide, live vaccines Adverse effects [6]
Alopecia (2–5%)
Pregnancy category: B
Important contra-indications noted in the Cardiovascular
Angina (2%)
prescribing guidelines for: nursing mothers
Hypertension (2–13%)
ANIDULAFUNGIN
Thrombophlebitis (2–5%) Trade names: Ecalta (Pfizer), Eraxis (Pfizer)
Central Nervous System
Fever (pyrexia) (12%) Central Nervous System Indications: Candidemia, candidal esophagitis
Headache (12–14%) [2] Carpal tunnel syndrome [2] Class: Antimycobacterial; echinocandin
Depression (5–13%) Half-life: 40–50 hours
Gastrointestinal/Hepatic Headache (9–13%) [2] Clinically important, potentially hazardous
Abdominal pain (5%) Pain (14%) interactions with: none known
Diarrhea (8%) Tumor pain (>5%) Pregnancy category: C
Nausea (8%)
Vomiting (14%) Endocrine/Metabolic Important contra-indications noted in the
Mastodynia (2–5%) prescribing guidelines for: nursing mothers;
Local pediatric patients
Injection-site edema [2] Gastrointestinal/Hepatic
Injection-site erythema [3] Diarrhea [2]
Injection-site inflammation [2] Hepatitis [2] Skin
Injection-site pain [4] Hepatotoxicity / liver injury / acute liver Angioedema (<2%)
Injection-site reaction (71%) [32] injury / drug-induced liver injury (DILI) [6] Erythema (<2%)
Nausea (11–19%) Flushing / rubefaction (<2%) [2]
Neuromuscular/Skeletal Vomiting (8–13%) Hot flashes (<2%)
Arthralgia (6–12%) Hyperhidrosis (<2%)
Genitourinary
Respiratory Vaginal dryness (2%) [3] Peripheral edema (11%)
Flu-like syndrome (6%) Pruritus (itching) (<2%)
Nasopharyngitis (12%) Neuromuscular/Skeletal
Ulcerations (5%)
Sinusitis (7%) Arthralgia (2–5%) [8]
Urticaria / hives (<2%)
Upper respiratory tract infection (4%) [2] Asthenia / fatigue (19%) [7]
Back pain (12%) [2] Mucosal
Other Bone or joint pain (6–11%) [2] Oral candidiasis (5%)
Adverse effects [6] Joint disorder [3] Cardiovascular
Death [2] Myalgia/Myopathy (2–5%) [2] Atrial fibrillation (<2%)
Infection (40%) [11] Osteoporosis (11%) Bundle branch block (<2%)
Respiratory Chest pain (5%)
Cough (11%) Hypertension (12%)
Flu-like syndrome (7%) Hypotension (15%)
Pharyngitis (6–14%) Phlebitis [2]
Other Thrombophlebitis (<2%)
Venous thromboembolism (10%)
Infection (2–5%)
Central Nervous System
Confusion (8%)
Depression (6%)
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 23
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
24 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 25
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Endocrine/Metabolic Cardiovascular
ALT increased [2] Hypertension (2%) APROTININ
Appetite decreased [2] Hypotension (6%) Trade name: Trasylol (Bayer)
Weight loss (10–12%) [7] Central Nervous System Indications: For prophylactic use to reduce
Gastrointestinal/Hepatic Anorexia (6–10%) [3] blood loss in patients undergoing coronary artery
Abdominal pain (<2%) [4] Encephalopathy [2] bypass surgery
Diarrhea (8–9%) [39] Fever (pyrexia) (3–6%) Class: Antifibrinolytic, Serine protease inhibitor
Dyspepsia / functional dyspepsia / Headache (5–9%) [6] Half-life: 150 minutes
gastroparesis [2] Insomnia (2–3%) Clinically important, potentially hazardous
Gastrointestinal disorder / discomfort [2] Somnolence (drowsiness) [2] interactions with: captopril, enalapril, lisinopril,
Nausea (7–9%) [39] Vertigo / dizziness (3–7%) [2] quinapril
Vomiting (<3%) [11] Endocrine/Metabolic Pregnancy category: B
Neuromuscular/Skeletal ALT increased (6%) Important contra-indications noted in the
Arthralgia [2] AST increased (3%) prescribing guidelines for: nursing mothers;
Asthenia / fatigue [5] Creatine phosphokinase (CPK) / creatine pediatric patients
Respiratory kinase increased (hyperCKemia) (4%) Warning: ANAPHYLACTIC OR
Nasopharyngitis (<3%) [21] Dehydration (6%) ANAPHYLACTOID REACTIONS
Upper respiratory tract infection (<4%) Gastrointestinal/Hepatic
[17] Abdominal pain (5%) [3] Skin
Other Constipation (9–10%) [9] Anaphylactoid reactions / anaphylaxis
Adverse effects [6] Diarrhea (<10%) [3] (includes anaphylactic shock) [25]
Infection [2] Dyspepsia / functional dyspepsia / Hypersensitivity [4]
gastroparesis (5–6%) Lipohypertrophy [2]
Flatulence (4%) Peripheral edema (5%)
APREPITANT Gastritis / gastric irritation (4%) Rash (2%)
Nausea (6–13%) Cardiovascular
Trade name: Emend (Merck) Vomiting (3–8%) Arrhythmias (3–4%)
Indications: Prevention of postoperative and Genitourinary Atrial fibrillation (21%)
chemotherapy induced nausea and vomiting
Urinary tract infection (2%) Atrial flutter (6%)
Class: Antiemetic, CYP3A4 inhibitor, Neurokinin
Hematologic Cardiac failure (5%)
1 receptor antagonist
Anemia (3%) Chest pain (2%)
Half-life: 9–13 hours
Febrile neutropenia [3] Extrasystoles (6%)
Clinically important, potentially hazardous
Neutropenia (neutrophils decreased) (3–6%) Hypertension (4%)
interactions with: alprazolam, antifungal agents,
[4] Hypotension (8%)
astemizole, avanafil, betamethasone,
Local Myocardial infarction (6%)
carbamazepine, cisapride, clarithromycin, Pericarditis (5%)
colchicine, conivaptan, corticosteroids, CYP2C9 Infusion-related reactions [2]
Infusion-site pain [2] Phlebitis (1–10%)
substrates, CYP3A4 inducers or inhibitors, Pulmonary edema / cardiogenic pulmonary
dasatinib, deferasirox, dexamethasone, diltiazem, Neuromuscular/Skeletal edema (<2%)
docetaxel, eplerenone, estrogens, everolimus, Asthenia / fatigue (5–18%) [10] Supraventricular tachycardia (4%)
fentanyl, grapefruit juice, halofantrine, ifosfamide, Otic Tachycardia (6%)
imatinib, irinotecan, itraconazole, ketoconazole, Tinnitus (4%) Ventricular tachycardia (5%)
methylprednisolone, midazolam, mifepristone, Renal Central Nervous System
naldemedine, nefazodone, neratinib, olaparib, Proteinuria (7%) Confusion (4%)
oral contraceptives, paroxetine hydrochloride, Other Fever (pyrexia) (15%)
phenobarbital, phenytoin, pimecrolimus, Hiccups (11%) [9] Insomnia (3%)
pimozide, progestins, ranolazine, rifampin, Infection [3]
rifamycin derivatives, rifapentine, ritonavir,
Endocrine/Metabolic
Creatine phosphokinase (CPK) / creatine
salmeterol, saxagliptin, St John’s wort,
kinase increased (hyperCKemia) (2%)
telithromycin, terfenadine, tolbutamide, APROBARBITAL Gastrointestinal/Hepatic
tolvaptan, trabectedin, triamcinolone,
troleandomycin, vinblastine, vincristine, Trade name: Alurate (Roche) Constipation (4%)
voriconazole, warfarin Indications: Short-term sedation, sleep induction Diarrhea (3%)
Pregnancy category: N/A (Insufficient evidence Class: Barbiturate Nausea (11%)
to inform drug-associated risk) Half-life: 14–34 hours Vomiting (3%)
Important contra-indications noted in the Clinically important, potentially hazardous Genitourinary
prescribing guidelines for: nursing mothers; interactions with: alcohol, brompheniramine, Urinary retention (3%)
pediatric patients buclizine, dicumarol, ethanolamine, warfarin Urinary tract infection (2%)
Note: Fosaprepitant is a prodrug of aprepitant Important contra-indications noted in the Hematologic
for injection. Aprepitant treatment is given along prescribing guidelines for: the elderly; nursing Anemia (2%)
with a 5-HT3-receptor antagonist and mothers; pediatric patients Thrombosis (<2%)
dexamethasone. Neuromuscular/Skeletal
Asthenia / fatigue (2%)
Skin Renal
Pruritus (itching) (8%) Nephrotoxicity / kidney injury / acute kidney
Hair injury (AKI) / drug-induced kidney injury [2]
Alopecia (12%) Renal failure (<2%)
Mucosal Renal function abnormal / renal dysfunction
Mucocutaneous reactions (3%) (3%)
Stomatitis (oral mucositis) (3%) Respiratory
Asthma (2%)
26 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 27
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Hypertension [3]
QT prolongation [2] ARISTOLOCHIA ARSENIC
Central Nervous System Family: Aristolochiaceae Synonyms: Arsenic trioxide (Trisenox);
Agitation (19%) [5] Scientific names: Aristolochia clematitis, Potassium arsenite solution (Fowler’s solution)
Akathisia (8–13%) [38] Aristolochia serpentaria Trade name: Trisenox (Cephalon)
Anxiety (17%) [11] Indications: Aphrodisiac, anti-allergy, Indications: Acute promyelocytic leukemia,
Compulsions [2] anticonvulsant, promotes menstruation psoriasis (in the early 1900s), devitalization of
Dyskinesia [3] Class: Immunomodulator pulp in dental procedures
Extrapyramidal symptoms [11] Half-life: N/A Class: Antineoplastic, Trace element
Fever (pyrexia) (2%) Clinically important, potentially hazardous Half-life: 10–14 hours
Headache (27%) [14] interactions with: none known Clinically important, potentially hazardous
Hypersexuality [2] Pregnancy category: N/A interactions with: abacavir, acetazolamide,
Impulse control disorder [4] Note: Aristolochia has been reported to cause alfuzosin, aloe vera (gel, juice, leaf), amiodarone,
Insomnia (18%) [22] severe kidney damage or ‘Chinese herb amitriptyline, amphotericin B, artemether/
Irritability [5] nephropathy’. Eighteen patients developed lumefantrine, bretylium, chloroquine,
Mania [2] carcinomas of the bladder, ureter and/or renal chlorpromazine, ciprofloxacin, clomipramine,
Neuroleptic malignant syndrome [14] pelvis. clozapine, disopyramide, diuretics, dronedarone,
Neurotoxicity [2] Aristolochia is banned in the European Union and droperidol, enoxacin, erythromycin, fluphenazine,
Parkinsonism [12] Japan. gadobutrol, garlic, gatifloxacin, ginger, ginseng,
Psychosis [2]
haloperidol, indacaterol, levofloxacin,
Restlessness [10]
Skin levomepromazine, lithium, lomefloxacin,
Schizophrenia (exacerbation) [2]
Carcinoma [2] mesoridazine, moxifloxacin, nilotinib, norfloxacin,
Sedation [12]
Skin toxicity / toxicity [2] ofloxacin, phenothiazines, pimozide,
Somnolence (drowsiness) (5–11%) [14]
Stroke / cerebral infarction [2] Renal procainamide, prochlorperazine, promethazine,
Suicidal ideation [6] Nephrotoxicity / kidney injury / acute kidney QT prolonging antipsychotics, quetiapine,
Tardive dyskinesia [8] injury (AKI) / drug-induced kidney injury [9] quinidine, quinine, quinolones, sotalol,
Tic disorder [3] sparfloxacin, tetrabenazine, thioridazine,
Tremor (3%) [9] toremifene, trifluoperazine, vandetanib,
Vertigo / dizziness [8]
ARMODAFINIL vemurafenib, ziprasidone, zuclopenthixol
Pregnancy category: D
Endocrine/Metabolic Trade name: Nuvigil (Cephalon)
Important contra-indications noted in the
Appetite increased [5] Indications: Narcolepsy, obstructive sleep prescribing guidelines for: nursing mothers;
Diabetes mellitus [2] apnea, shift work sleep disorder
pediatric patients
Galactorrhea [2] Class: Eugeroic Warning: APL DIFFERENTIATION SYNDROME
Hyperprolactinemia [2] Half-life: 12–15 hours and ECG ABNORMALITIES
SIADH [2] Clinically important, potentially hazardous
Weight gain (2–30%) [33] interactions with: cyclosporine
Gastrointestinal/Hepatic Pregnancy category: C Skin
Important contra-indications noted in the Basal cell carcinoma [5]
Constipation (11%) [5]
prescribing guidelines for: the elderly; nursing Bowen’s disease [6]
Dyspepsia / functional dyspepsia /
mothers; pediatric patients Bruise / bruising / contusion / ecchymosis
gastroparesis (9%)
(ecchymoses) (20%)
Nausea (15%) [14]
Bullous dermatosis [4]
Vomiting (11%) [6] Central Nervous System Carcinoma [20]
Genitourinary Anxiety [2] Dermatitis (43%) [6]
Priapism [3] Headache (14–23%) [10] Edema (40%) [2]
Urinary retention [2] Insomnia (4–6%) [3] Erythema (13%)
Vaginitis [2] Vertigo / dizziness (5%) [2] Erythema multiforme [4]
Hematologic Gastrointestinal/Hepatic Exanthems [5]
Neutropenia (neutrophils decreased) [5] Diarrhea [3] Exfoliative dermatitis (5%) [7]
Local Nausea [2] Facial edema (8%)
Injection-site pain [8] Other Fixed eruption [2]
Neuromuscular/Skeletal Adverse effects [2] Flushing / rubefaction (10%)
Asthenia / fatigue [5] Gangrene [2]
Ataxia [4] Herpes simplex (13%)
Dystonia [13]
ARNICA Herpes zoster (8%) [4]
Pisa syndrome (pleurothotonus) [2] Hyperhidrosis (13%)
Family: Asteraceae; Compositae Hyperkeratosis (palms and soles) (40%) [5]
Ocular Scientific names: Arnica fulgens, Arnica montana, Hypersensitivity (5%)
Vision blurred (3–8%) Arnica sororia Keratoses [20]
Renal Indications: Bruising, aches and sprains, insect Leukomelanosis [7]
Enuresis [3] bites, superficial phlebitis, diuretic, flavoring Lymphadenopathy (8%)
Respiratory agent, found in hair tonic and shampoo Melanoma [5]
Cough (3%) Class: Immunomodulator Melanosis / melanocytosis [6]
Nasopharyngitis [2] Half-life: N/A Merkel cell carcinoma [4]
Upper respiratory tract infection [3] Clinically important, potentially hazardous Pallor (10%)
interactions with: none known Palmar–plantar desquamation [16]
Other Pregnancy category: N/A
Adverse effects [6] Palmar–plantar hyperhidrosis [2]
Death [3] Palmar–plantar hyperkeratosis [20]
Hiccups [4] Skin Palmar–plantar punctate keratoses [2]
Toothache [2] Dermatitis [5] Petechiae (8%)
Pigmentation (8%) [15]
Pityriasis rosea (from organic arsenic) [2]
28 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Pruritus (itching) (33%) Pancreatitis / acute pancreatitis [2] azithromycin, carbamazepine, ciprofloxacin,
Purpura (20%) Vomiting (58%) [2] citalopram, clomipramine, conivaptan, CYP2D6
Squamous cell carcinoma [15] Genitourinary substrates, CYP3A4 inducers, inhibitors or
Stevens-Johnson syndrome [3] Oliguria (5%) substrates, darunavir, dasatinib, degarelix,
Urticaria / hives (8%) Urinary incontinence (5%) delavirdine, disopyramide, dolasetron, duloxetine,
Xerosis (15%) Vaginal bleeding (13%) flecainide, halofantrine, hormonal contraceptives,
Hair Hematologic imipramine, indinavir, itraconazole, lapatinib,
Alopecia [4] Anemia (20%) levofloxacin, levomepromazine, lopinavir,
Nails Bleeding (8%) mefloquine, moxifloxacin, nelfinavir, norfloxacin,
Leukonychia striata (Mees’ lines) [3] Febrile neutropenia (13%) ofloxacin, paroxetine hydrochloride, pazopanib,
Nail pigmentation [2] Leukocytosis (elevated white blood cell phenytoin, pimozide, procainamide, quinidine,
Mucosal (WBC) count) (50%) quinine, rifampin, risperidone, sotalol, St John’s
Epistaxis (nosebleed) (25%) Neutropenia (neutrophils decreased) (10%) wort, telavancin, telithromycin, terfenadine,
Oral candidiasis (5%) [2] tipranavir, venlafaxine, voriconazole, vorinostat,
Oral mucosal eruption (8%) [3] Sepsis (5%) ziprasidone, zuclopenthixol
Xerostomia (dry mouth) (8%) Thrombocytopenia (18%) Pregnancy category: C
Local Important contra-indications noted in the
Cardiovascular
Injection-site edema (10%) prescribing guidelines for: nursing mothers;
Arrhythmias [2]
Injection-site erythema (13%) pediatric patients
Chest pain (25%)
Injection-site pain (20%) Note: Artemether/Lumefantrine tablets should
Hypertension (10%)
not be used to treat severe malaria or to prevent
Hypotension (25%) Neuromuscular/Skeletal
malaria.
Palpitation (10%) Arthralgia (33%)
QT prolongation (40%) [10] Asthenia / fatigue (63%)
Tachycardia (55%) Back pain (18%) Skin
Torsades de pointes [3] Bone or joint pain (23%) Abscess (<3%)
Central Nervous System Myalgia/Myopathy (25%) Impetigo (<3%)
Agitation (5%) Neck pain (13%) Inflammation [3]
Anorexia (23%) Osteonecrosis [7] Pruritus (itching) (4%) [2]
Anxiety (30%) Pain in extremities (13%) Rash (3%) [6]
Coma (5%) Ocular Urticaria / hives (<3%) [2]
Confusion (5%) Eyelid edema (5%) Cardiovascular
Depression (20%) Ocular itching (10%) Palpitation (18%) [2]
Fever (pyrexia) (63%) Vision blurred (10%) Central Nervous System
Headache (60%) Xerophthalmia (8%) Agitation (<3%)
Insomnia (43%) Otic Anorexia (40%) [6]
Neurotoxicity [2] Ear pain (8%) Chills (23%)
Pain (15%) Tinnitus (5%) Fever (pyrexia) (25–29%) [6]
Paresthesias (33%) Renal Gait instability (<3%)
Pseudotumor cerebri [2] Renal failure (8%) Headache (56%) [9]
Rigors (38%) Hypoesthesia (numbness) (<3%)
Seizures (8%) Respiratory Insomnia (5%) [2]
Somnolence (drowsiness) (8%) Cough (65%) Mood changes (<3%)
Tremor (13%) Dyspnea / shortness of breath (53%) Seizures [2]
Vertigo / dizziness (23%) Hemoptysis (8%) Sleep disturbances (22%)
Hypoxia (23%) Sleep-related disorder [2]
Endocrine/Metabolic Nasopharyngitis (5%)
Acidosis (including lactic acidosis) (5%) Tremor (<3%)
Pharyngolaryngeal pain (35%) Vertigo / dizziness (39%) [9]
ALT increased (20%) Pleural effusion (20%)
Appetite decreased (15%) Rhonchi (8%) Endocrine/Metabolic
AST increased (13%) Sinusitis (20%) ALT increased (<3%)
Hyperglycemia (45%) Tachypnea / respiratory rate increased (8%) AST increased (<3%)
Hyperkalemia (18%) Upper respiratory tract infection (13%) Hypokalemia (<3%)
Hypocalcemia (10%) Wheezing (13%) Gastrointestinal/Hepatic
Hypoglycemia (8%) Abdominal pain (17%) [12]
Hypokalemia (50%) Other
Death [3] Constipation (<3%)
Hypomagnesemia (45%) Diarrhea (8%) [12]
Weight gain (13%) Dyspepsia / functional dyspepsia /
Weight loss (8%) ARTEMETHER/ gastroparesis (<3%)
Gastrointestinal/Hepatic Dysphagia (<3%)
Abdominal distension (8%) LUMEFANTRINE Gastroenteritis (<3%)
Abdominal pain (58%) Hepatomegaly (6–9%)
Black stools (8%) Trade name: Coartem (Novartis) Nausea [8]
Constipation (28%) [2] Indications: Acute, uncomplicated malaria Peptic ulceration (<3%)
Diarrhea (53%) infections due to Plasmodium falciparum in Vomiting [17]
Dyspepsia / functional dyspepsia / patients of 5kg bodyweight and above
Class: Antimalarial Genitourinary
gastroparesis (10%) Hematuria (<3%)
Fecal incontinence (8%) Half-life: ~2 hours (artemether); 3–6 days
(lumefantrine) Urinary tract infection (<3%)
Gastrointestinal bleeding (8%) Hematologic
Hepatotoxicity / liver injury / acute liver Clinically important, potentially hazardous
interactions with: amiodarone, amitriptyline, Anemia (4–9%) [4]
injury / drug-induced liver injury (DILI) [3] Eosinophilia (<3%)
Loose stools (10%) amoxapine, antimalarials, antiretrovirals, arsenic,
astemizole, atazanavir, atovaquone/proguanil, Hemolytic anemia [2]
Nausea (75%) [2] Neutropenia (neutrophils decreased) [2]
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 29
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
30 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 31
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
cocoa mixes, coffee beverages, frozen desserts, Lichenoid eruption [2] Skin
gelatin desserts, juice beverages, laxatives, Pityriasis rosea [3] Urticaria / hives [2]
multivitamins, milk drinks, pharmaceuticals and Pruritus (itching) [6] Mucosal
supplements, shake mixes, soft drinks, tabletop Psoriasis [3] Xerostomia (dry mouth) [4]
sweeteners, tea beverages, instant teas and Purpura [8] Cardiovascular
coffees, topping mixes, wine coolers, yogurt. Rash (<10%) Arrhythmias [2]
Stevens-Johnson syndrome [6] QT prolongation [10]
Skin Toxic epidermal necrolysis [9] Torsades de pointes [10]
Angioedema [2] Urticaria / hives (<10%) [72]
Vasculitis (angiitis) / cutaneous vasculitis Central Nervous System
Panniculitis [3] Paresthesias [3]
Urticaria / hives [4] (angiitis) [2]
Somnolence (drowsiness) [3]
Other Mucosal
Allergic reactions [2] Aphthous stomatitis / aphthous ulcer /
aphtha (aphthae) [3] ASTRAGALUS ROOT
Epistaxis (nosebleed) [2]
ASPIRIN Nasal polyp [4] Family: Fabaceae; Leguminosae
Oral mucosal eruption [3] Scientific names: Astragalus membranaceus,
Synonyms: acetylsalicylic acid; ASA Oral ulceration (see also aphthous stomatitis Astragalus mongholicus
Trade names: Aggrenox (Boehringer Ingelheim), / aphthous ulcer / aphtha) [4] Indications: Arrhythmia, colds, upper
Anacin (Wyeth), Ascriptin (Novartis) (Wallace), Central Nervous System respiratory infections, chronic fatigue syndrome,
Darvon Compound (aaiPharma), Durlaza (New Stroke / cerebral infarction [2] colitis, diabetes, hepatitis, hypotension, herpes
Haven), Ecotrin (GSK), Equagesic (Women First), simplex keratitis
Excedrin (Bristol-Myers Squibb), Fiorinal Gastrointestinal/Hepatic
Class: Antioxidant, Immune stimulant,
(Watson), Norgesic (3M), Soma Compound Black stools [3]
Vasodilator
(MedPointe), Talwin Compound (Sanofi-Aventis), Gastritis / gastric irritation [2]
Half-life: N/A
Yosprala (Aralez) Gastrointestinal bleeding [8]
Gastrointestinal ulceration [7] Clinically important, potentially hazardous
Indications: Pain, fever, inflammation interactions with: none known
Class: Antiplatelet, Non-steroidal anti- Hepatotoxicity / liver injury / acute liver
injury / drug-induced liver injury (DILI) [4] Pregnancy category: N/A
inflammatory (NSAID), Salicylate
Half-life: 15–20 minutes Pancreatitis / acute pancreatitis [2]
Clinically important, potentially hazardous Hematologic ATAZANAVIR
interactions with: acemetacin, acenocoumarol, Bleeding [17]
amitriptyline, anagrelide, anticoagulants, azficel-t, Ocular Trade names: Evotaz (Bristol-Myers Squibb),
bismuth, calcium hydroxylapatite, capsicum, Periorbital edema [3] Reyataz (Bristol-Myers Squibb)
celecoxib, cholestyramine, cilazapril, citalopram, Indications: HIV infection
Otic
desvenlafaxine, devil’s claw, dexamethasone, Class: Antiretroviral, HIV-1 protease inhibitor
Tinnitus [17]
dexibuprofen, dichlorphenamide, diclofenac, Half-life: 7 hours
Renal Clinically important, potentially hazardous
dicumarol, duloxetine, enoxaparin, etodolac, Fanconi syndrome [2]
evening primrose, flunisolide, flurbiprofen, ginkgo interactions with: abiraterone, alfuzosin,
Respiratory amiodarone, antacids, aripiprazole, artemether/
biloba, ginseng, heparin, ibuprofen, iloprost,
Asthma [10] lumefantrine, atorvastatin, avanafil, bepridil,
indomethacin, ketoprofen, ketorolac, Pulmonary toxicity [2]
lumiracoxib, meloxicam, methotrexate, methyl bosentan, buprenorphine, cabazitaxel,
Rhinitis [3] cabozantinib, calcifediol, cisapride,
salicylate, methylprednisolone, milnacipran, Sinusitis [2]
nilutamide, NSAIDs, paroxetine hydrochloride, clarithromycin, colchicine, crizotinib,
phellodendron, piroxicam, prednisone,
Other cyclosporine, darifenacin, dasatinib,
Adverse effects [9] dexlansoprazole, diltiazem, dofetilide, efavirenz,
resveratrol, reteplase, rivaroxaban, sermorelin,
Allergic reactions [2] elbasvir & grazoprevir, eluxadoline, ergot
sulfites, tinzaparin, tirofiban, tolmetin,
triamcinolone, urokinase, valdecoxib, valproic derivatives, erlotinib, estrogens, etravirine,
everolimus, famotidine, felodipine, fentanyl,
acid, venlafaxine, verapamil, vilazodone, warfarin, ASTEMIZOLE fesoterodine, flibanserin, fluticasone propionate,
zafirlukast
Pregnancy category: D Trade name: Histeamen (Janssen) garlic, glecaprevir & pibrentasvir, indinavir,
Important contra-indications noted in the Indications: Urticaria, pruritus, allergic rhinitis irinotecan, itraconazole, ixabepilone,
prescribing guidelines for: nursing mothers; Class: Histamine H1 receptor antagonist ketoconazole, lapatinib, lidocaine, lopinavir,
pediatric patients Half-life: 20 hours lovastatin, maraviroc, marihuana, midazolam,
Note: NSAIDs may cause an increased risk of Clinically important, potentially hazardous mifepristone, naldemedine, nevirapine,
serious cardiovascular and gastrointestinal interactions with: amiodarone, aprepitant, nicardipine, nifedipine, olaparib, ombitasvir/
adverse events, which can be fatal. This risk may artemether/lumefantrine, azithromycin, bepredil, paritaprevir/ritonavir, omeprazole, oral
increase with duration of use. bosentan, bretylium, cisapride, clarithromycin, contraceptives, paclitaxel, pantoprazole,
Aggrenox is aspirin and dipyridamole; Yosprala is darunavir, dasatinib, delavirdine, disopyramide, pazopanib, pimozide, posaconazole, proton-
aspirin and omeprazole. erythromycin, erythromycin fluconazole, pump inhibitors, quetiapine, quinidine, quinine,
fluoxetine, fluvoxamine, grapefruit juice, indinavir, rabeprazole, raltegravir, ranolazine, rifabutin,
Skin itraconazole, ketoconazole, metronidazole, rifampin, rilpivirine, ritonavir, rivaroxaban,
Anaphylactoid reactions / anaphylaxis miconazole, nefazodone, nilotinib, paroxetine romidepsin, rosuvastatin, salmeterol, saquinavir,
(includes anaphylactic shock) (<10%) [8] hydrochloride, pimozide, probucol, sildenafil, simeprevir, simvastatin, sirolimus,
Angioedema (<5%) [32] procainamide, quinidine, quinine, ritonavir, sofosbuvir/velpatasvir/voxilaprevir, solifenacin,
Bullous dermatosis [4] saquinavir, sertindole, sertraline, sotalol, SSRIs, sonidegib, St John’s wort, sunitinib, tacrolimus,
Erythema multiforme [9] terfenadine, troleandomycin, voriconazole, tadalafil, telaprevir, telithromycin, temsirolimus,
Erythema nodosum [9] zileuton, ziprasidone tenofovir disoproxil, ticagrelor, tipranavir,
Erythroderma [2] Pregnancy category: C trazodone, triazolam, tricyclic antidepressants,
Exanthems [11] Note: Hismanal has been withdrawn in the USA vardenafil, vemurafenib, verapamil, voriconazole,
Fixed eruption [22] as of 1999. warfarin
Hypersensitivity [5] Pregnancy category: B
32 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
Important contra-indications noted in the Important contra-indications noted in the Important contra-indications noted in the
prescribing guidelines for: the elderly; nursing prescribing guidelines for: the elderly; nursing prescribing guidelines for: nursing mothers;
mothers; pediatric patients mothers; pediatric patients pediatric patients
Note: Evotaz is atazanavir and cobicistat. Note: Contra-indicated in patients with sinus
bradycardia, heart block greater than first degree, Skin
Skin cardiogenic shock, or overt cardiac failure. Beta- Peripheral edema (18%)
Jaundice (5–7%) [11] Adalat and Tenif are atenolol and nifedipine. Pruritus (itching) (13%) [6]
Rash (3–20%) [7] Kalten, Tenoret 50 and Tenoretic are atenolol and Rash (15%) [7]
chlorthalidone. Chlorthalidone is a sulfonamide
Cardiovascular Cardiovascular
and can be absorbed systemically. Sulfonamides
QT prolongation [2] Hypertension [2]
can produce severe, possibly fatal, reactions such
Torsades de pointes [2] Venous thromboembolism (>2%)
as toxic epidermal necrolysis and Stevens-Johnson
Central Nervous System syndrome. Central Nervous System
Depression (2%) Warning: CESSATION OF THERAPY Encephalitis [8]
Fever (pyrexia) (2%) Fever (pyrexia) (21%) [4]
Headache (<6%) [3] Endocrine/Metabolic
Insomnia (3%) Skin
Anaphylactoid reactions / anaphylaxis ALP increased (4%)
Neurotoxicity [2] ALT increased (2%) [3]
Pain (3%) (includes anaphylactic shock) [2]
Lupus erythematosus [2] Appetite decreased (26%) [7]
Vertigo / dizziness (3%) AST increased (2%) [6]
Necrosis / skin necrosis [3]
Endocrine/Metabolic Pruritus (itching) (<5%) Dehydration (>2%)
ALT increased (3%) Psoriasis [7] Diabetes mellitus [2]
AST increased (3%) Raynaud’s phenomenon [2] Diabetic ketoacidosis [3]
Creatine phosphokinase (CPK) / creatine Urticaria / hives [2] Hyperglycemia (5%)
kinase increased (hyperCKemia) (8%) Hyperthyroidism (2%)
Hyperbilirubinemia [7] Cardiovascular Hyponatremia (10%) [2]
Atrial fibrillation (5%) [2] Hypothyroidism (6%) [3]
Gastrointestinal/Hepatic Atrial flutter (2%)
Abdominal pain (4%) Serum creatinine increased (3%)
Bradycardia / sinus bradycardia (3–18%) [8]
Cholelithiasis (gallstones in the gallbladder) Cardiac arrest (2%) Gastrointestinal/Hepatic
[4] Cardiac failure (19%) Abdominal pain (17%)
Diarrhea (2%) [3] Heart block (5%) Colitis [6]
Hepatotoxicity / liver injury / acute liver Hypotension (25%) [2] Constipation (21%) [2]
injury / drug-induced liver injury (DILI) [3] Postural hypotension (12%) Diarrhea (18%) [4]
Nausea (6–14%) [4] Supraventricular tachycardia (12%) Gastric obstruction (>2%)
Vomiting (3–4%) Ventricular tachycardia (16%) Hepatitis [3]
Genitourinary Nausea (25%) [6]
Central Nervous System Vomiting (17%)
Urolithiasis [4] Depression (12%)
Hematologic Somnolence (drowsiness) (2%) Genitourinary
Neutropenia (neutrophils decreased) (5%) Stroke / cerebral infarction [2] Hematuria (14%)
Neuromuscular/Skeletal Syncope / fainting [2] Urinary tract infection (22%)
Asthenia / fatigue (2%) Vertigo / dizziness (15%) Hematologic
Back pain (2%) Gastrointestinal/Hepatic Anemia (8%) [4]
Myalgia/Myopathy (4%) Diarrhea (3%) Lymphopenia (lymphocytopenia) (10%)
Renal Nausea (3%) Sepsis (>2%)
Nephrolithiasis [5] Neuromuscular/Skeletal Local
Nephrotoxicity / kidney injury / acute kidney Asthenia / fatigue (26%) Infusion-related reactions (3%)
injury (AKI) / drug-induced kidney injury [7] Leg pain (3%) Neuromuscular/Skeletal
Respiratory Respiratory Arthralgia (14%) [2]
Upper respiratory tract infection [2] Dyspnea / shortness of breath (6%) Asthenia / fatigue (52%) [12]
Other Wheezing (3%) Back pain (15%)
Adverse effects [5] Myalgia/Myopathy [2]
Other Neck pain (15%)
Infection (~50%) Adverse effects [5]
Renal
Nephrotoxicity / kidney injury / acute kidney
ATENOLOL ATEZOLIZUMAB injury (AKI) / drug-induced kidney injury
(>2%)
Trade names: Beta-Adalat (Bayer), Kalten (BPC), Trade name: Tecentriq (Genentech) Respiratory
Tenif (AstraZeneca), Tenoret 50 (AstraZeneca), Indications: Locally advanced or metastatic Cough (14%) [2]
Tenoretic (AstraZeneca), Tenormin urothelial carcinoma in patients having disease Dyspnea / shortness of breath (16%) [4]
(AstraZeneca) progression following platinum-containing Hypoxia [2]
Indications: Angina, hypertension, acute chemotherapy, bladder cancer, non-small cell lung Pneumonia (>2%) [2]
myocardial infarction cancer Pneumonitis (3%) [3]
Class: Antiarrhythmic class II, Beta adrenergic Class: Immune checkpoint inhibitor, Monoclonal
blocker, Beta blocker antibody, Programmed death-ligand (PD-L1)
Other
Half-life: 6–7 hours (adults) Adverse effects [8]
inhibitor
Clinically important, potentially hazardous Infection (38%)
Half-life: 27 days
interactions with: alfuzosin, calcium channel Clinically important, potentially hazardous
blockers, cisplatin, clonidine, digitalis glycosides, interactions with: none known
diltiazem, disopyramide, epinephrine, Pregnancy category: N/A (Can cause fetal
indomethacin, reserpine, verapamil harm)
Pregnancy category: D
Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC 33
derm_www - 18/8/2021 09:16 [v1.0]
Proof [[1] derm #1] by
34 Litt’s Drug Eruption & Reaction Manual B 2022 by Taylor & Francis Group, LLC
Another random document with
no related content on Scribd:
leaders demanded of Andros that he surrender both his office and
himself. The man refused and fled to his stronghold, whence he
defied the patriots and continued to the last to declare his power,
though like water now fast escaping from his grasp.
Surrounding their ex-master they made him a prisoner, not a
refugee, and at length he gave in and was captured and sent to
confinement, along with the others of his recent government.
With an instinct for conventions, the citizens were soon
assembled. Howsoever great had been their heat in their moment of
rebellion and triumph, they were calm enough to be wise when the
time arrived to declare for themselves. They reinstated Bradstreet
and the Council of ’86. They declared the old Government in force
and their former charter ipso facto restored, unimpaired by the
interim of nearly three years of maladministration.
William and Mary received the report of all these swiftly terminated
proceedings with a favor which was not unblended with
astonishment. Admiring the Protestant spirit, which it had become
their own special province to uphold, they lost no time in confirming
the entire course of actions, even to the temporary resumption of
their old charter privileges and powers, by the patriots across the
sea. And there, for a time, they were contented to permit the matter
to rest. The affairs of England they had found so completely
engrossing that they had no time to spare toward regranting a
specific charter to Massachusetts.
Increase Mather, suspicions of privileges and liberties not
absolutely signed, sealed and delivered, remained at his post,
working continuously and sedulously to obtain that monarchical
support and confirmation of the colony’s prerogatives which his
many compatriots had sent him to secure.
Sir William Phipps, on the other hand, realized the busy state of
mind in which William and Mary had been so abruptly plunged, and
he therefore deferred further work with Mather for a time more
suitable. Then, when he learned that the French Catholics in
America had formed alliances with the Indians and were already
overrunning the Protestant territory and committing daily
depredations, he made up his mind once more to return to the field
of action, in which he might be able to render more effective service
than he could by remaining in England.
He arrived in the summer of that fateful year, ’89, and offered
himself to Bradstreet at once. The period of warfare in which he
thereupon engaged was one of great length and of much bitterness.
Alternating defeat and victory left the advantages with the French
and Indians, so far as hopes of ultimate success were concerned.
The colonists had to make such long, tedious marches that decisive
victories for their arms were almost impossible. The enemy gained in
confidence, audacity and numbers.
In despair the General Court finally offered two sloops of war, free,
together with all the profits of plunder which might result from the
enterprise, to any man who would undertake to reduce to ashes
Penobscot, St. John’s and Port Royal, the seats of the French and
Indian power. The offer attracted Phipps, who foresaw, in the
execution of the task, an infinite amount of adventure and action.
He enlisted men for the undertaking. Yet matters grew worse with
such alarming rapidity that before the enterprise could be placed in
readiness for work, it became necessary to raise a small fleet of
vessels prepared for war-like operations. Thus seven sloops and
seven hundred men, under command of Sir William, sailed away to
the North on their sinister errand.
Port Royal, secure and arrogant, in her fancied isolation from
attack, was surprised and taken. The French were routed with great
loss. The town was looted until hardly so much as a sauce-pan was
left by the thorough-going warriors of New England. The plunder,
while not enormously valuable, nevertheless was sufficient to help
materially in meeting the expenses of the venture. But its indirect
effect on the colonists was not so happy. Cupidity is so often the
jackal that follows righteous indignation.
The Puritans foresaw opportunities to punish the enemy, at the
enemy’s own expense. A second expedition, to go against Quebec,
was planned, the patriots expecting in confidence that, like the first, it
would surely succeed, if Phipps were at its head, and that the
plunder would more than repay the initial expenses of the expedition.
Sir William, having expressed his doubts of the wisdom of this
over-ambitious scheme, nevertheless commanded the fleet once
more as it sailed away, eager for further conquest.
The enterprise was doomed to failure from the first. It dragged out
interminably, it developed jealousies, it was ill-planned. Such a
bedraggled, failure-smitten lot of lame-duck sloops returned to
Boston that the council were simply appalled. They had expended so
much of their meager hoard of funds on the venture, that the
treasury was practically bankrupted.
Blame rained upon the head of Phipps, for not having succeeded
against impossible conditions. Driven to extremities, by the woeful
lack of plunder, the colony-fathers were obliged, for the first time in
their history, to issue paper currency. The notes ranged in value from
denominations of two shillings up to ten pounds.
Still an undimmed patriot, ready to serve his country in whatsoever
direction an opportunity was afforded, Williams Phipps gave his gold
for the colony’s bills, absorbing thus a very considerable sum. His
example induced investments in the paper from all directions.
Nevertheless the currency soon came tumbling down in value, till a
pound in paper was worth less than three-fourths of its face.
The sailors, and other working people, lost heavily, in these times
of trouble and weakened confidence. Yet eventually the money was
all redeemed at par by the Massachusetts government.
Sir William, weary of being reviled for his pains, returned to
England once again and resumed his labors with Increase Mather, to
secure to the colony a definite charter.
CHAPTER V.
OLD ACQUAINTANCES.
A BEEF-EATER PASSES.