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Your healthcare professionals (e.g., doctor or pharmacist) may already be aware of any possible drug
interactions and may be monitoring you for it. Do not start, stop or change the dosage of any
medicine before checking with them first.
Storage
Store at or below 77 degrees F (25 degrees C) in a dry place away from light and moisture. Do not
store in the bathroom. Keep all medicines away from children and pets.
Nursing Responsibilities
-Instruct the patient to refer to the health care professionals if the symptoms worsen
-Assess the client’s history
Administration
Prior to initiating therapy, confirm the diagnosis of hypogonadism by ensuring that serum
testosterone concentrations have been measured in the morning on at least two separate days and
that these serum testosterone concentrations are below the normal range
Adverse Effects
Abnormal dreams, Acne, Anaphylaxis, Bladder irritability, Breast soreness, Cholestatic jaundice, Deep
vein thrombosis, Dry skin, Fatigue, Gynecomastia, Headache, Insomnia, Menstrual irregularities,
Priapism, Suppression of factors II, V, VII and Virilization
Pregnancy
Contraindicated in pregnant women; drug is teratogenic and may cause fetal harm when
administered to a pregnant woman based on data from animal studies and its mechanism of action;
exposure of female fetus to androgens may result in varying degrees of virilization
Action
Endogenous androgen; promotes growth and development of male sex organs and maintains
secondary sex characteristics in androgen-deficient males
Uses
This medicated patch contains testosterone. It is used for hormone replacement in men who are not
able to produce enough testosterone (for example, due to hypogonadism). This medication is
absorbed through the skin, enters your bloodstream, and helps your body reach normal
testosterone levels.
Nurse responsibilities
- Read the Patient Information Leaflet provided by the pharmacist before start using testosterone
and each time get a refill.
-Notice the client for any questions, and llow the patient if needs for products for the skin and allow
the patient to know the undesirable effects
- Read the dosing instructions carefully for each product. Do not change products without prefer
doctor or pharmacist
-Instruct the patient about the dosages, If any symptoms may occur inform immediately.
Side Effects
Itching, irritation, and discomfort at the application site may occur during the first few days as your
body adjusts to the patch. Other side effects may include acne, headache, hair loss, anxiety, and a
change in sexual desire.
STORAGE:
Store patches in their protective pouches at room temperature away from heat, light and moisture.
Do not store in the bathroom.
Side Effects
·diarrhea, excitation, restlessness,
·trouble sleeping (insomnia), or
·breast swelling in men.
Dosage
The recommended daily dose of Anadrol-50 in children and adults is 1-5 mg/kg body weight per day.
The usual effective dose is 1-2 mg/kg/day but higher doses may be required, and the dose is
individualized. Response is not often immediate, and three to six months should be given
INDICATIONS
treatment of anemias caused by deficient red cell production. Acquired aplastic anemia, congenital
aplastic anemia, myelofibrosis and the hypoplastic anemias due to the administration of myelotoxic
drugs often respond.
ANADROL Tablets should not replace other supportive measures such as transfusion, correction of
iron, folic acid, vitamin B12 or pyridoxine deficiency, antibacterial therapy and the appropriate use of
corticosteroids.
DOSAGE AND ADMINISTRATION
The recommended daily dose in children and adults is 1-5 mg/kg body weight per day. The usual
effective dose is 1-2 mg/kg/day but higher doses may be required, and the dose should be
individualized. Response is not often immediate, and a minimum trial of three to six months should
be given. Following remission, some patients may be maintained without the drug; others may be
maintained on an established lower daily dosage. A continued maintenance dose is usually
necessary in patients with congenital aplastic anemia.
DRUG INTERACTIONS
Warfarin: Clinically significant pharmacokinetic and pharmacodynamic interactions between anabolic
steroids and warfarin have been reported in healthy volunteers. When anabolic steroid therapy is
initiated in a patient already receiving treatment with warfarin, the INR
(international normalized ratio) or prothrombin time (PT) should be monitored closely and the dose
of warfarin adjusted as necessary until a stable target INR or PT has been achieved. Furthermore, in
patients receiving both ANADROL Tablets and warfarin, careful monitoring of the INR or PT and
adjustment of the warfarin dosage, if indicated, are recommended when the ANADROL dose is
changed or discontinued. Patients should be closely monitored for signs and symptoms of occult
bleeding.
Anticoagulants: Anabolic steroids may increase sensitivity to oral anticoagulants. Dosage of the
anticoagulant may have to be decreased in order to maintain the desired prothrombin time. Patients
receiving oral anticoagulant therapy require close monitoring, especially when anabolic steroids are
started or stopped.
Drug/Laboratory Test Interferences
Therapy with androgenic anabolic steroids may decrease levels of thyroxine-binding globulin
resulting in decreased total T4 serum levels and increased resin uptake of T3 and T4. Free thyroid
hormone levels remain unchanged and there is no clinical evidence of thyroid dysfunction. Altered
tests usually persist for 2 to 3 weeks after stopping anabolic therapy.
CONTRAINDICATIONS
Carcinoma of the prostate or breast in male patients., Carcinoma of the breast in females with
hypercalcemia;, androgenic anabolic steroids may stimulate osteolytic resorption of bones,
Oxymetholone can cause fetal harm when administered to pregnant women. It is contraindicated in
women who are or may become pregnant. If the patient becomes pregnant while taking the drug,
she should be apprised of the potential hazard to the fetus, Nephrosis or the nephrotic phase of
nephritis, Hypersensitivity to the drug andSevere hepatic dysfunction.
·Anavar (oxandrolone)
·Dianabol (methandienone )
·Winstrol (stanozolol)
·Restandol (testosterone undecanoate)
Indication
In patients with significant renal disease and hepatic dysfunction, maximum dose is 2 g/day. In
patients receiving intermittent hemodialysis, give 1 to 2 I.V. every 24 hours after dialysis session.
Administration
-Before giving drug, ensure patient is not allergic to penicillins or cephalosporins
-Obtain specimen for culture and sensitivity tests before giving first dose. Begin therapy while
awaiting results
Adverse Reaction
-Skin: Pain, induration, tenderness at injection site and rash
-Other: Hypersensitivity reactions, serum sickness, anaphylaxis
Interactions
Aminoglycosides: May increase nephrotoxicity and cause synergestic effect against some strains of
Pseudomonas aeruginosa and Enterobateriaceae species
Contraindication
-Patients with hypersensitive to drug or other cephalosporins
-Use cautiously in patients hypersensitive to penecilin because of possibility of cross-sensitivity with
other beta-lactum antibiotics
Nurse Responsibilities
-Monitor for patients for superinfection, diarrhea, and anemia and treat appropriately
-Tell the patient to report adverse reaction promptly
-Instruct patient to report discomfort at I.V.
-Tell patient to notify prescriber about loose stools or diarrhea
K. Nutritional Supplements
Brand Name: Enervon Activ
Generic Name:ascorbic acid + calcium carbonate + colecalciferol
Uses: Nutritional supplement to help promote optimum physical & mental performance.
Side effects Nicotinamide (>100 mg/day): Flushing of the face, arms & chest. Fe (doses of elemental
Fe >120 mg/day): GI effects eg, nausea, vomiting, bloating & upper abdominal discomfort. Ginseng
(high doses >3 g/day): HTN, nervousness, insomnia, edema, diarrhea & skin reactions. Royal jelly:
Hypersensitivity reactions eg, eczema, rhinitis, urticaria & bronchospasm.
Nursing responsibilities: make sure to educate patient on taking this as it says on the instruction
label
Drug Interactions
Ginseng: May enhance the effect of oral hypoglycemics (eg, glimepiride, glipizide). Decreased effect
of MAOIs (eg, selegiline, phenelzine, moclobemide. Decreased blood prothrombin levels w/ warfarin.
Dosage/Direction for Use
1-2 softgel cap daily.
Contraindications
Hypersensitivity. Pregnancy & lactation.
Brand Name: Appebon with Iron Capsule
Generic Name: Buclizine HCl 25 mg, vit B1 10 mg, vit B6 5 mg, vit B12 10 mcg, elemental Fe
25 mg (as Fe fumarate 76 mg)
Uses: Nutritional supplement in patients w/ depressed appetite.
Side effects: May impair ability to drive or operate machinery.
Nursing responsibilities: make sure to educate patient on taking this as it says on the instruction
label
Drug Interactions
May potentiate CNS depressant effect of barbiturates, tranquilizers & alcohol.
Dosage/Direction for Use
1 cap daily.
Special Precautions
May impair ability to drive or operate machinery.
L. Immunizing Agents
Brand Name: Benadryl AB
Generic name: Diphenhydramine
Indications/Uses
Perennial & seasonal (hay fever) allergic rhinitis; vasomotor rhinitis, allergic conjunctivitis due to
inhalant allergens & foods; amelioration of allergic reactions to blood or plasma, dermatographism;
adjunct to epinephrine for anaphylactic reactions after acute manifestations have been controlled.
Active treatment & prophylaxis for motion sickness & parkinsonism.
Dosage/Direction for Use
Adult 50 mg tid-qid. Childn >20 lb 12.5-25 mg tid-qid. Max: 300 mg/day. Base on body wt: 5 mg/kg/24
hr. Motion sickness To be taken 30 min before exposure to motion.
Administration
May be taken with or without food.
Nursing responsibilities: make sure patient is comfortable and aware with contraindications like
hypersensitivity
Adverse Reactions
Urticaria, drug rash, anaphylactic shock, photosensitivity, excessive perspiration, chills, dryness of
mouth, nose & throat; hypotension, headache, palpitations, tachycardia, extrasystoles; hemolytic
anemia; thrombocytopenia, agranulocytosis; sedation, sleepiness, dizziness, disturbed coordination,
fatigue, confusion, restlessness, excitation, nervousness, tremor, irritability. Insomnia, euphoria,
paresthesia, blurred vision, diplopia, vertigo, tinnitus, acute labyrinthitis. Hysteria, neuritis,
convulsions; epigastric distress, anorexia, nausea, vomiting, diarrhea, constipation; urinary frequency,
difficult urination, urinary retention, early menses; thickening of bronchial secretions, tightness of
chest & wheezing nasal stuffiness.
Drug Interactions
Increased effects w/ alcohol & other CNS depressants (hypnotics, sedatives, tranquilizers). Prolonged
& intensified anticholinergic effects w/ MAOIs. Prolonged & intensified anticholinergic effects w/
MAOIs.
ATC Classification
R06AA02 - diphenhydramine ; Belongs to the class of aminoalkyl ethers used as systemic
antihistamines.