When to Administer Adipex (Phentermine)
Adipex can be prescribed for patients with BMI ≥30 kg/m² or BMI ≥27 kg/m² with weight-related comorbidities (hypertension, type 2 diabetes, dyslipidemia, obstructive sleep apnea), but only after excluding cardiovascular disease and other absolute contraindications. 1, 2
Patient Selection Criteria
BMI Requirements
- Prescribe phentermine for patients with BMI ≥30 kg/m² without comorbidities 1, 2
- Prescribe for patients with BMI ≥27 kg/m² who have weight-related comorbidities including hypertension, type 2 diabetes, dyslipidemia, or obstructive sleep apnea 1
Absolute Contraindications (Never Prescribe)
- Any history of cardiovascular disease including coronary artery disease, stroke, arrhythmias, congestive heart failure, or uncontrolled hypertension 1, 3, 2
- Current or recent (within 14 days) monoamine oxidase inhibitor (MAOI) use due to risk of hypertensive crisis 4, 2
- Pregnancy or nursing 1, 4, 2
- Hyperthyroidism 4, 2
- Glaucoma 4, 2
- Agitated states or anxiety disorders 4, 2
- History of drug abuse 2
- Known hypersensitivity to sympathomimetic amines 2
Pre-Treatment Assessment
Required Screening Before First Dose
- Measure baseline blood pressure and heart rate 4
- Screen for cardiovascular disease history through detailed history 4
- Assess pregnancy status in all females of reproductive potential and provide contraception counseling 4
- Exclude hyperthyroidism 4
- Screen for glaucoma 4
- Evaluate for agitated states or anxiety disorders 4
- Confirm no MAOI use in past 14 days 4
- Assess renal function (eGFR) 2
Renal Dosing Adjustments
- Maximum dose 15 mg daily for severe renal impairment (eGFR 15-29 mL/min/1.73 m²) 2
- Avoid phentermine entirely in end-stage renal disease (eGFR <15 mL/min/1.73 m²) or dialysis patients 2
Dosing and Administration
Standard Dosing
- Start with 15 mg orally once daily, taken approximately 2 hours after breakfast 2
- May increase to 30 mg daily if needed for adequate appetite suppression 2
- Alternative low-dose regimen: 8 mg up to three times daily (at 1:00 PM and 4:00 PM) to target afternoon/evening eating patterns 4, 5
- Avoid late evening dosing due to insomnia risk 2
- Not recommended for patients under 16 years of age 2
Duration of Treatment
- FDA-approved only for short-term use (up to 12 weeks) 4, 2
- Many practitioners prescribe off-label for longer durations given obesity's chronic nature, but this requires ongoing monitoring 4, 3
- Discontinue if <5% weight loss after 12 weeks on maximum dose 1, 4, 3
Monitoring Requirements
Initial Phase (First 3 Months)
- Monitor blood pressure and heart rate at every visit, at least monthly 1, 4
- Assess efficacy and safety monthly 1
Ongoing Monitoring (Beyond 3 Months)
- Continue blood pressure and heart rate monitoring at every visit 3
- Assess weight loss progress at least every 3 months 1
- Monitor for side effects including dry mouth, insomnia, dizziness, irritability, nausea, constipation 1, 4
Special Populations to Avoid
Cardiovascular Risk Patients
- Do not prescribe phentermine to patients with any cardiovascular disease 1, 3
- Consider orlistat as a safer alternative for patients with cardiovascular concerns, as it works via gastrointestinal lipase inhibition rather than sympathetic activation 1, 4
- Lorcaserin is another safer alternative for cardiovascular patients (though note: lorcaserin was withdrawn from market in 2020) 1
Drug Interaction Concerns
- Avoid combining with other sympathomimetic agents 2, 6
- Do not combine with serotonergic agents (SSRIs like fluoxetine, sertraline, paroxetine) due to lack of safety data 2
- Exercise caution with tramadol (severe drug-drug interaction potential) 6
- Avoid combination with dextromethorphan (moderate interaction) 6
Patient Counseling Points
Setting Expectations
- Phentermine must be combined with lifestyle modifications including reduced-calorie diet, exercise, and behavioral therapy—never use as monotherapy 1, 2
- Inform patients of FDA approval for short-term use only (12 weeks), though off-label longer use is common 4, 3
- Explain that phentermine is a Schedule IV controlled substance, though addiction potential is low when used appropriately 1, 7
Warning Signs Requiring Immediate Discontinuation
- New or worsening dyspnea (potential primary pulmonary hypertension) 2
- Angina pectoris 2
- Syncope 2
- Lower extremity edema 2
Common Pitfalls to Avoid
- Do not prescribe to patients with "stable" or "controlled" cardiovascular disease—any cardiovascular history is an absolute contraindication 1, 3
- Do not continue beyond 12 weeks if inadequate weight loss (<5%) achieved 1, 4, 3
- Do not prescribe late in the day due to insomnia risk 2
- Do not combine with other weight loss medications or serotonergic agents 2
- Do not overlook renal function assessment—dose adjustment required for renal impairment 2