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DRUG STUDY (Quetiapine) - SANGUYO, CB.
DRUG STUDY (Quetiapine) - SANGUYO, CB.
Name of the Patient : _______Sabrina _____________ Age : __26 y.o____ Sex : __Female__ Name of Student _________Sanguyo, Camille B. ____
Civil Status : _____ Single________Religion : _____ N/A_____ Rm/Bed No. _________________ Area : ____NCMH ___________ Level/ Block : _Level III-B______
Address : _____________________ N/A ______________________ Date Submitted : ________March 08, 2022_______________
Date of Admission : _____________________________ Diagnosis : Factitious Disorder (FD) Rating : ___________________________________________________
MEDICATION Classification/ Action Indications Contraindications Side Effects Adverse Effects Nursing Responsibilities
Generic Name: Pharmacotherapeutic class: Treatment This drug is contraindicated Frequent (19%–10%): Overdose may produce: Before:
of acute manic episodes to patients with: Dizziness Heart block
Quetiapine Dibenzodiazepine derivative associated with bipolar Drowsiness Hypotension Verify the doctor’s order regarding
disorder (alone or in Hypersensitivity to Headache Hypokalemia the medication.
Brand Name: Clinical class: combination with lithium quetiapine Observe the ten rights of
Tachycardia
or valproate). Occasional (9%–3%): medication administration.
--- Second-generation Use cautiously in:
Treatment of acute Constipation Assess behavior, appearance,
(atypical) antipsychotic
Usual Dosage/Frequency: depressive episodes Orthostatic emotional status, response to
Hepatic/renal
Action: associated with bipolar hypotension environment, speech pattern,
impairment
Initial: 25 mg twice daily on day Antagonizes dopamine and disorder. Tachycardia thought content.
1. Increased by 25 to 50 twice serotonin Preexisting abnormal Dry mouth Assess for suicidal tendencies,
daily or three times a day on (anti-psychotic activity), lipid profile Dyspepsia especially during early therapy.
days 2 and 3. histamine (somnolence), Rash Restrict amount of drug available
Usual: 300 to 400 mg daily by alpha1-adrenergic Patients at risk for to patient.
Asthenia
day 4, in divided doses twice (orthostatic hypotension) aspiration pneumonia, Assess daily weight and BMI.
cardiovascular disease Abdominal pain
daily or three times a day. receptors. Obtain serum potassium, LFT,
(e.g., HF, history of MI) Rhinitis
Increased every 2 days in CBC and renal function tests.
increments of 25 to 50 mg Therapeutic effect: Rare (2%): Question for history of allergies
Cerebrovascular
twice daily, as needed. Diminishes symptoms Back pain and full medication history; screen
disease
Maximum: 800 mg daily associated with
Fever for interactions.
schizophrenia/bipolar Dehydration Educate and verify patient and
Weight gain
disorders. SO’s understanding about the
Pharmacokinetics: Hypovolemia medication.
Usual Route:
History of drug Check the medication three times.
Absorption:
Oral Well absorbed after oral abuse/dependence, Obtain baseline vital signs.
administration Obtain baseline I&O.
Drug Order: Seizure disorder
Distribution: During:
Quetiapine 200mg three times Widely distributed in tissues; Hypothyroidism
a day CNS concentration exceeds Maintain patient’s comfort and
Patients at risk for
plasma concentration suicide safety.
Drug Interactions: Administer the drug: Quetiapine
Protein binding: 83% Parkinson’s disease 200mg three times a day, as
Concurrent use of
macrolide anti-infectives ordered by the physician.
Metabolism: Decreased GI motility
(erythromycin, May be administered without
Extensively metabolized by
clarithromycin), dofetilide, Urinary retention regard to food. Extended-release
the liver (mostly by P450
sotalol, quinidine, tablets should be swallowed
CYP3A4 enyzme
disopyramide, Narrow-angle whole, do not break, crush, or
system)
procainamidethioridazine, glaucoma chew.
chlorpromazine, Elimination: If therapy is reinstituted after an
Diabetes interval of 1 week off, follow initial
droperidol, gemifloxacin, < 1% excreted unchanged
moxifloxacin, mefloquine, in the urine titration schedule.
Visual problems
pentamidine, arsenic Monitor BP (sitting, standing,
trioxide, dolasetron, Half-life: Elderly lying) and pulse before and
citalopram, 6 hours frequently during initial dose
escitalopramtacrolimus, Patients at risk for titration. If hypotension occurs
and ziprasidone increase Pharmacodynamics: orthostatic hypotension during dose titration, return to the
the risk of serious Onset: Unknown previous dose.
Peak: Unknown Avoid use in patients at
ventricular arrhythmias Observe patient carefully when
Duration: 12 hours risk for torsades de
and should be avoided. administering to ensure
pointes (hypokalemia,
medication is swallowed and not
hypomagnesemia,
Increased CNS hoarded or cheeked.
history of cardiac
depression may occur with
arrhythmias, congenital After:
alcohol, antihistamines,
long QT syndrome,
opioid analgesics, and
concurrent medications Assess for hypersensitivity
sedative/hypnotics.
that prolong QT reaction (chills, fever).
Increased risk of interval). Monitor CBC, LFT, hepatic
hypotension with acute enzyme levels, etc.
ingestion of alcohol or Monitor for onset of
antihypertensives. extrapyramidal side effects
(akathisia, restlessness; dystonia,
Phenytoin and thioridazine or pseudo-parkinsonism). Report
increase clearance and these symptoms if present.
decrease effectiveness of Monitor for tardive dyskinesia
quetiapine (dose change (involuntary rhythmic movement of
may be necessary); mouth, face, and extremities).
similar effects may occur Report immediately; may be
with carbamazepine, irreversible.
barbiturates, rifampin, Monitor for development of
corcorticosteroids. neuroleptic malignant syndrome
(fever, respiratory distress,
Effects may be increased tachycardia, seizures, etc.). Notify
by ketoconazole, health care professional
itraconazole, fluconazole, immediately if these symptoms
protease inhibitors or occur.
erythromycin, as well as Monitor for symptoms related to
by other agents that inhibit hyperprolactinemia (menstrual
the cytochrome P450 abnormalities, galactorrhea,
CYP3A4 enzyme sexual dysfunction).
Evaluate the drug’s desired
therapeutic effect: decrease in
excited, manic, behavior, positive
and negative symptoms.
Monitor for side/adverse effects.
Document medication
administration properly as per
institution’s protocol.
Patient/Family Teaching:
References:
Vallerand, A. H., Sanoski, C. A., & Deglin, J. H. (2013). Davis’s Drug Guide for Nurses (13th ed.). F.A. Davis Company. 1079-1081.
Kizior, R. J., & Hodgson, K. J. (2020). Saunders Nursing Drug Handbook 2021 (1st ed.). Elsevier. 983-985.
Jones & Bartlett Learning. (2015). 2021 Nurse’s Drug Handbook (14th ed.). Jones & Bartlett Learning. 1018-1020.