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Phentermine Hydrochloride 37.5 mg

Dosage: 37.5 mg

Imprints: “ADIPEX-P” “37.5”

Shapes /Colors : Blue & White Capsules

Manufacturer: TEVA.

Delivery time:
Within USA: 24 to 48 hours
Canada: 2 to 3 Days
International Delivery: 3 to 5 Days

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DOSAGE FORMS AND STRENGTHS
Capsules: (phentermine mg/topiramate mg extended-release)
3.75 mg/23 mg
7.5 mg/46 mg
11.25 mg/69 mg
15 mg/92 mg
Dosage should be individualized to obtain an adequate response with the lowest effective dose. The usual adult dose is one capsule (37.5 mg) daily as prescribed by the physician, administered before breakfast or 1 to 2 hours after breakfast for appetite control. The usual adult dose is one tablet (37.5 mg) daily, as prescribed by the physician, administered before breakfast or 1 to 2 hours after breakfast. The dosage may be adjusted to the patient’s need. For some patients, half tablet (18.75 mg) daily may be adequate, while in some cases it may be desirable to give half tablets (18.75 mg) two times a day. ADIPEX-P® is not recommended for use in pediatric patients less or equal 16 years of age.

Contraindications

ADIPEX-P® is contraindicated for use in any patient with a prior history of sympathomimetic amine hypersensitivity or idiosyncratic reaction to sympathomimetic amines.(e.g., coronary artery disease, stroke, arrhythmias, congestive heart failure, uncontrolled hypertension)
During or within 14 days following the administration of monoamine oxidase inhibitors
Hyperthyroidism
Glaucoma
Agitated states
History of drug abuse
Pregnancy
Nursing
Known hypersensitivity or idiosyncrasy to the sympathomimetic amines

Side Effects

Common side effects
Blurry vision
Dry mouth
Constipation
Nausea
Irritability
Airway infection above the lungs
Inflammation of nose and throat
Back pain
Headache
Dizziness
Trouble sleeping

Warnings

  • Fetal Toxicity: Females of reproductive potential: Obtain negative
    pregnancy test before treatment and monthly thereafter; use
    effective contraception. Qsymia is available through a limited
    the program under a Risk Evaluation and Mitigation Strategy (REMS)
    • Increase in Heart Rate: Monitor heart rate in all patients, especially
    those with cardiac or cerebrovascular disease.
    • Suicidal Behavior and Ideation: Monitor for depression or suicidal
    thoughts. Discontinue Qsymia if symptoms develop.
    • Acute Myopia and Secondary Angle Closure Glaucoma:
    Discontinue Qsymia.
    • Mood and Sleep Disorders: Consider dose reduction or withdrawal
    for clinically significant or persistent symptoms.
    • Cognitive Impairment: May cause disturbances in attention or
    memory. Caution patients about operating automobiles or
    hazardous machinery when starting treatment.
    • Metabolic Acidosis: Measure electrolytes before/during treatment.
    • Elevated Creatinine: Measure creatinine before/during treatment.
    • Use of Antidiabetic Medications: Weight loss may cause
    hypoglycemia. Measure serum glucose before/during treatment. Wikifor more info on Adipex.

 

Additional information

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