Clonidine Hydrochloride description, usages, side effects, indications, overdosage, supplying and lots more!

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Clonidine Hydrochloride

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

CLONIDINE HYDROCHLORIDE DESCRIPTION




Clonidine Hydrochloride




CLINICAL PHARMACOLOGY






PHARMACOKINETICS





INDICATIONS & USAGE


CLONIDINE HYDROCHLORIDE CONTRAINDICATIONS

PRECAUTIONS).

WARNINGS

Withdrawal


Because children commonly have gastrointestinal illnesses that lead to vomiting, they may be particularly susceptible to hypertensive episodes resulting from abrupt inability to take medication.

PRECAUTIONS

General





Perioperative Use

INFORMATION FOR PATIENTS




DRUG INTERACTIONS



Toxicology).

TOXICOLOGY




CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY



PREGNANCY



CLINICAL PHARMACOLOGY, Pharmacokinetics). Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

NURSING MOTHERS


PEDIATRIC USE

WARNINGS, Withdrawal).

CLONIDINE HYDROCHLORIDE ADVERSE REACTIONS



Body as a Whole:Fatigue, fever, headache, pallor, weakness, and withdrawal syndrome. Also reported were a weakly positive Coombs' test and increased sensitivity to alcohol.
Cardiovascular:Bradycardia, congestive heart failure, electrocardiographic abnormalities (i.e., sinus node arrest, junctional bradycardia, high degree AV block and arrhythmias), orthostatic symptoms, palpitations, Raynaud's phenomenon, syncope, and tachycardia. Cases of sinus bradycardia and atrioventricular block have been reported, both with and without the use of concomitant digitalis.
Central Nervous System:Agitation, anxiety, delirium, delusional perception, hallucinations (including visual and auditory), insomnia, mental depression, nervousness, other behavioral changes, paresthesia, restlessness, sleep disorder, and vivid dreams or nightmares.
Dermatological:Alopecia, angioneurotic edema, hives, pruritus, rash, and urticaria.
Gastrointestinal:Abdominal pain, anorexia, constipation, hepatitis, malaise, mild transient abnormalities in liver function tests, nausea, parotitis, pseudo-obstruction (including colonic pseudo-obstruction), salivary gland pain, and vomiting.
Genitourinary:Decreased sexual activity, difficulty in micturition, erectile dysfunction, loss of libido, nocturia, and urinary retention.
Hematologic:Thrombocytopenia.
Metabolic:Gynecomastia, transient elevation of blood glucose or serum creatine phosphokinase, and weight gain.
Musculoskeletal:Leg cramps and muscle or joint pain.
Oro-otolaryngeal:Dryness of the nasal mucosa.
Ophthalmological:Accommodation disorder, blurred vision, burning of the eyes, decreased lacrimation, and dryness of eyes.

OVERDOSAGE




DOSAGE & ADMINISTRATION

Adults


Initial Dose


Maintenance Dose


Renal Impairment

HOW SUPPLIED






STORAGE AND HANDLING




PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Clonidine Hydrochloride



Clonidine Hydrochloride

Clonidine Hydrochloride

clonidine hydrochloride TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:52125-038(NDC:53489-215)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CLONIDINE HYDROCHLORIDE clonidine 0.1 mg

Inactive Ingredients

Ingredient Name Strength
ALUMINUM OXIDE
cellulose, microcrystalline
D&C YELLOW NO. 10
LACTOSE
MAGNESIUM STEARATE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics

Color Size Imprint Code Shape
yellow 7 mm MP;657 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52125-038-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA070925 2012-08-20


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Be sure to consult your doctor before taking any medication!
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