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Guanidine


General


Pronunciation

(GWAHN i deen)


Indications


Use: Labeled Indications

Reduction of the symptoms of muscle weakness associated with the myasthenic syndrome of Eaton-Lambert, not for myasthenia gravis


Contraindications


Hypersensitivity to guanidine or any component of the formulation


Dosing and Administration


Dosing: Adult

Eaton-Lambert syndrome: Oral: Initial: 10-15 mg/kg/day in 3-4 divided doses, gradually increase to 35 mg/kg/day, or up to development of side effects


Dosing: Geriatric

Refer to adult dosing.


Dosing: Renal Impairment

No dosage adjustment provided in manufacturer 's labeling.


Dosing: Hepatic Impairment

No dosage adjustment provided in manufacturer 's labeling.


Storage

Store at 25 ‚ °C (77 ‚ °F); excursions permitted to 15 ‚ °C to 30 ‚ °C (59 ‚ °F to 86 ‚ °F).


Dosage Forms/Strengths


Dosage Forms

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Tablet, Oral, as hydrochloride:

Generic: 125 mg


Drug Interactions

Acetylcholinesterase Inhibitors: May enhance the adverse/toxic effect of Cholinergic Agonists. Monitor therapy

Beta-Blockers: May enhance the adverse/toxic effect of Cholinergic Agonists. Of particular concern are the potential for cardiac conduction abnormalities and bronchoconstriction. Management: Administer these agents in combination with caution, and monitor for conduction disturbances. Avoid methacholine with any beta blocker due to the potential for additive bronchoconstriction. Monitor therapy

Cimetropium: Cholinergic Agonists may diminish the anticholinergic effect of Cimetropium. Monitor therapy


Monitoring Parameters

CBC with differential (baseline and frequently thereafter); creatinine, BUN, urinalysis


Adverse Reactions


Frequency not defined.

Cardiovascular: Atrial fibrillation, cold extremities, flushing, hypotension, palpitations, tachycardia

Central nervous system: Ataxia, confusion, dizziness, emotional lability, hallucination, irritability, jitteriness, mood changes, nervousness, psychosis

Dermatologic: Diaphoresis, folliculitis, paresthesia, skin rash, xeroderma

Gastrointestinal: Abdominal cramps, anorexia, diarrhea, gastric irritation, nausea, sore throat, xerostomia

Genitourinary: Uremia

Hematologic & oncologic: Anemia, bone-marrow depression, bruise, leukopenia, petechia, purpura, thrombocytopenia

Hepatic: Abnormal hepatic function tests

Neuromuscular & skeletal: Tremor

Renal: Increased serum creatinine, interstitial nephritis (acute or chronic), renal tubular necrosis

Miscellaneous: Fever


Warnings/Precautions


Concerns related to adverse effects:

- Bone marrow suppression: Dose-related, fatal bone marrow suppression had been reported with use. Avoid concurrent use with medications known to suppress bone marrow. Monitor closely; discontinue use if bone marrow suppression is suspected.

Disease-related concerns:

- Renal impairment: Use with caution in patients with renal impairment.


Pregnancy Considerations

Animal reproduction studies have not been conducted.


Patient and Family Education


Patient Education

- Discuss specific use of drug and side effects with patient as it relates to treatment. (HCAHPS: During this hospital stay, were you given any medicine that you had not taken before? Before giving you any new medicine, how often did hospital staff tell you what the medicine was for? How often did hospital staff describe possible side effects in a way you could understand?)

- Patient may experience abdominal pain, flushing, sweating a lot, lack of appetite, nausea, diarrhea, abdominal cramps, or dry mouth. Have patient report immediately to prescriber signs of infection, signs of kidney problems (urinary retention, blood in urine, change in amount of urine passed, or weight gain), behavioral changes, severe dizziness, passing out, burning or numbness feeling, change in balance, tremors, confusion, mood changes, hallucinations, arrhythmia, or tachycardia (HCAHPS).

- Educate patient about signs of a significant reaction (eg, wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat). Note: This is not a comprehensive list of all side effects. Patient should consult prescriber for additional questions.

Intended Use and Disclaimer: Should not be printed and given to patients. This information is intended to serve as a concise initial reference for healthcare professionals to use when discussing medications with a patient. You must ultimately rely on your own discretion, experience and judgment in diagnosing, treating and advising patients.

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