Phentermine (Adipex-P) Tablets - Uses, Dosage, MOA, Side effects

Phentermine (Ionamin, Adipex) is a stimulant drug that is used in the short-term treatment for weight loss adjunct to diet, exercise, and behavioral therapy.

Phentermine (Adipex-P) Uses:

  • Obesity (short-term adjunct):
    • It is indicated for the short-term treatment of weight loss as an adjunct to diet, exercise, and behavioral therapy in patients with an initial body mass index (BMI) ≥30 kg/m² or ≥27 kg/m² and comorbid conditions such as diabetes, dyslipidemia, and controlled hypertension.

Phentermine is recommended in combination with topiramate for weight loss. It is available by the brand name of Qsymia. The other five weight loss pills recommended by the AACE and ACE are:

  1. Orlistat (Xenical)
  2. Liraglutide (Victoza)
  3. Lorcaserin (Belviq) - Recently withdrawn because of carcinogenic effects
  4. Naltrexone ER/ Bupropion ER (Contrave)
  5. Phentermine/ Topiramate (Qsymia)

Phentermine (Adipex-P) Dose in Adults

 Note:

  • In the US, Suprenza has been withdrawn for more than a year.
  • In terms of the salt, phentermine hydrochloride, dosing is described (not as phentermine base).

Phentermine (Adipex-P) Dose in the short-term treatment of Obesity as an adjunct to diet and behavioral therapy:

  • Capsule, tablet (excluding Lomaira):
    • 15 to 37.5 mg/day in one or two divided doses.
    • The lowest effective dose should be used to achieve adequate response and minimal side effects.
  • Tablet (Lomaira only):
    • 8 mg thrice daily.
    • The lowest effective dose should be used to achieve adequate response and minimal side effects.
  • Orally disintegrating tablet (ODT):
    • One tablet 15 to 37.5 mg once a day in the morning.
    • The lowest effective dose should be used to achieve adequate response and minimal side effects.

Use in children:

Refer to adult dosing.   

Pregnancy Risk Factor X

  • It is not recommended for pregnant women.
  • Obesity has been linked to adverse fetal outcomes. Weight loss medication should be avoided during pregnancy.

Use of phentermine while breastfeeding

  • It is not recommended for lactating mothers.
  • It is unknown if the drug is excreted into breastmilk. Other amphetamines were detected in breastmilk.

Phentermine (Adipex-P) Dose in Kidney Disease:

Capsule, tablet (excluding Lomaira):

  • eGFR ≥30 mL/minute/1.73 m²:
    • It should be used with caution as the systemic exposure of the drug is increased. However, the manufacturer has not provided any adjustments in the dose.
  • eGFR 15 to 29 mL/minute/1.73 m²:
    • The maximum dose of 15 mg/day should not be exceeded.
  • eGFR <15 mL/minute/1.73 m²:
    • It has not been studied in severe kidney disease and should be avoided.
  • End-stage renal disease (ESRD) requiring dialysis:
    • It has not been studied in patients with ESRD and should be avoided.

Tablet (Lomaira only):

  • It should be used with caution as the systemic exposure of the drug is increased.
  • However, the manufacturer has not provided any adjustments in the dose as it has not been studied in patients with kidney disease.

Phentermine (Adipex-P) Dose in Liver disease:

  • It has not been studied in patients with liver disease.
  • Adjustments in the dose have not been provided by the manufacturer.   

Side effects of Phentermine (Adipex-P):

  • Cardiovascular:
    • Hypertension
    • Ischemia
    • Palpitations
    • Tachycardia
  • Central Nervous System:
    • Dizziness
    • Dysphoria
    • Euphoria
    • Headache
    • Insomnia
    • Overstimulation
    • Psychosis
    • Restlessness
  • Dermatologic:
    • Urticaria
  • Endocrine & Metabolic:
    • Change In Libido
  • Gastrointestinal:
    • Constipation
    • Diarrhea
    • Gastrointestinal Distress
    • Unpleasant Taste
    • Xerostomia
  • Genitourinary:
    • Impotence
  • Neuromuscular & Skeletal:
    • Tremor

Contraindications to Phentermine (Adipex-P):

  • Any phentermine, other sympathomimetic amines, or formulation component-related allergic reactions or idiosyncrasies;
  • a history of cardiovascular diseases 
  • hyperthyroidism;
  • glaucoma;
  • agitated states;
  • Past history of drug abuse;
  • Concomitant use or use within 14 days of an MAO inhibitor;
  • pregnancy;
  • breast-feeding

Warnings and Precautions

  • CNS effects
    • It may result in central nervous system depression, which may impair the patient's ability to do duties that call for mental acuity, such as operating heavy machinery or a vehicle.
  • Heart Failure:
    • The AHA has categorised it as a substance with a major potential for cardiac deterioration (AHA [Page 2016,]).
  • Primary pulmonary hypertension (PPH).
    • Rarely, phentermine has been linked to serious, sometimes fatal, pulmonary hypertension.
    • Combining fenfluramine and dexfenfluramine can increase the risk of developing pulmonary hypertension.
    • Stop treating patients with syncope, pedal edoema, or new-onset dyspnea or chest discomfort.
  • Heart disease of the valvular kind:
    • Combining phentermine with dexfenfluramine and fenfluramine can lead to serious regurgitant heart disease.
    • This affects primarily the mitral, Aortic, and Tricupid valves.
    • Rarely, phentermine is the only drug that has caused new-onset valvular heart disease.
  • Cardiovascular disease
    • Stimulant drugs can increase blood pressure and heart rate, which could lead to an exacerbation or worsening of existing heart disease and hypertension.
    • Patients with advanced cardiac conditions such as cardiomyopathy and rhythm abnormalities should avoid it.
  • Diabetes:
    • Hypoglycemia is more common in diabetic patients who have made dietary changes and used anorexiant medications.
    • Diabetic patients should be cautious when using the drug, and must adjust their anti-diabetic medication, especially insulin and/or sulfonylurea, to avoid hypoglycemia.
  • Renal impairment
    • Patients with kidney impairment are more likely to be exposed to drugs. This should be taken with caution.
    • It shouldn't be used in people with end-stage kidney disease who need hemodialysis or in those with severe renal impairment, such as those whose eGFR is fewer than 15 minutes.
  • Seizure disorders
    • Patients with a history or seizures should avoid it.
  • Tourette syndrome
    • Stimulant drugs can mask tics. Patients with Tourette syndrome should be cautious when using stimulants.

Phentermine: Drug Interaction

Note: Drug Interaction Categories:

  • Risk Factor C: Monitor When Using Combination
  • Risk Factor D: Consider Treatment Modification
  • Risk Factor X: Avoid Concomitant Use

Risk Factor C (Monitor therapy)

Alcohol (Ethyl)

May enhance the adverse/toxic effect of Phentermine.

Amifampridine

Amifampridine may have a stronger neuroexcitatory and/or seizure-potentiating impact when combined with substances with seizure threshold lowering potential.

Ammonium Chloride

May lower the level of amphetamines in the blood. This result is probably brought on by amphetamine excretion that is increased in the urine.

Antacids

Amphetamine excretion may be reduced.

Antihistamines

Antihistamines' sedative effects may be lessened by amphetamines.

Antihypertensive Agents

Amphetamines may reduce an antihypertensive agent's ability to lower blood pressure.

Antipsychotic Agents

May lessen amphetamines' stimulating effects.

Ascorbic Acid

May lower the level of amphetamines in the blood.

AtoMOXetine

Could make sympathomimetics' hypertensive effects stronger. The tachycardic impact of sympathomimetics may be increased by atoMOXetine.

BuPROPion

Agents With Seizure Threshold Lowering Potential may have an enhanced neuroexcitatory and/or seizure-potentiating impact.

Cannabinoid-Containing Products

Makes sympathomimetics' tachycardic effect stronger. Cannabidiol is an exception.

Carbonic Anhydrase Inhibitors

Amphetamine excretion may be reduced. Brinzolamide and dorzolamide are exceptions.

CYP2D6 Inhibitors (Moderate)

May raise the level of amphetamines in the blood.

CYP2D6 Inhibitors (Strong)

May increase the serum concentration of Amphetamines.

Doxofylline

Simpathomimetic drugs may intensify Doxofylline's harmful or hazardous effects.

Esketamine

Could make CNS stimulants' hypertensive effects more pronounced.

Ethosuximide

Ethosuximide's therapeutic effects may be lessened by amphetamines.Ethosuximide's serum levels may drop when amphetamines are consumed.

Gastrointestinal Acidifying Agents

May lower the level of amphetamines in the blood.

Guanethidine

Could make sympathomimetics more arrhythmogenic. Guanethidine might make sympathomimetic drugs more hypertensive.

Ioflupane I 123

Ioflupane I 123's ability to diagnose diseases may be compromised by amphetamines.

Lithium

May lessen amphetamines' stimulating effects.

Methenamine

May lower the level of amphetamines in the blood. This result is probably brought on by amphetamine excretion that is increased in the urine.

Multivitamins/Fluoride (with ADE)

May lower the level of amphetamines in the blood. More precisely, vitamin C, or ascorbic acid, which is present in many multivitamins, may lower amphetamine levels.

Multivitamins/Minerals (with ADEK, Folate, Iron)

May lower the level of amphetamines in the blood.

Multivitamins/Minerals (with AE, No Iron)

May lower the level of amphetamines in the blood. Specifically, vitamin C may make it harder for amphetamines to be absorbed.

Opioid Agonists

Opioid agonists' analgesic effects may be strengthened by amphetamines.

PHENobarbital

PHENobarbital's serum levels may be lowered by amphetamines.

Phenytoin

Phenytoin serum levels may be lowered by amphetamines.

Solriamfetol

Sympathomimetics may intensify Solriamfetol's hypertensive effects.

Solriamfetol

Solriamfetol's ability to cause hypertension may be enhanced by CNS stimulants.

Sympathomimetics

Could intensify the hazardous or harmful effects of other sympathomimetics.

Tedizolid

Could make sympathomimetics' hypertensive effects stronger. The tachycardic impact of sympathomimetics may be increased by tedizolid.

Tricyclic Antidepressants

Could make amphetamines more stimulating. Tricyclic antidepressants may potentially enhance amphetamines' cardiovascular effects.

Urinary Acidifying Agents

May lower the level of amphetamines in the blood.

Risk Factor D (Consider therapy modification)

Alkalinizing Agents

Amphetamine excretion may be reduced. Management: Take into account substitutes for the combination of amphetamines and alkalinizing agents. If these medications must be used concurrently, patients should be closely watched for any adverse effects from amphetamine usage.

Cocaine (Topical)

May enhance the hypertensive effect of Sympathomimetics. Management: Consider alternatives to use of this combination when possible. Monitor closely for substantially increased blood pressure or heart rate and for any evidence of myocardial ischemia with concurrent use.

Iohexol

Agents With Seizure Threshold Lowering Potential may enhance the adverse/toxic effect of Iohexol. Specifically, the risk for seizures may be increased. Management: Discontinue agents that may lower the seizure threshold 48 hours prior to intrathecal use of iohexol. Wait at least 24 hours after the procedure to resume such agents. In nonelective procedures, consider use of prophylactic anticonvulsants.

Iomeprol

Agents With Seizure Threshold Lowering Potential may enhance the adverse/toxic effect of Iomeprol. Specifically, the risk for seizures may be increased. Management: Discontinue agents that may lower the seizure threshold 48 hours prior to intrathecal use of iomeprol. Wait at least 24 hours after the procedure to resume such agents. In nonelective procedures, consider use of prophylactic anticonvulsants.

Iopamidol

Agents With Seizure Threshold Lowering Potential may enhance the adverse/toxic effect of Iopamidol. Specifically, the risk for seizures may be increased. Management: Discontinue agents that may lower the seizure threshold 48 hours prior to intrathecal use of iopamidol. Wait at least 24 hours after the procedure to resume such agents. In nonelective procedures, consider use of prophylactic anticonvulsants.

Linezolid

Could make sympathomimetics' hypertensive effects stronger. Reduce the first doses of sympathomimetic drugs and closely monitor individuals on linezolid for an augmented pressor response. There are currently no suggestions for specific dose adjustments.

Risk Factor X (Avoid combination)

Acebrophylline

Could make CNS stimulants more stimulating.

Iobenguane Radiopharmaceutical Products

Iobenguane radiopharmaceutical products' therapeutic effects may be reduced by amphetamines. Treatment: Before administering iobenguane, stop taking any medications that could impede or interfere with catecholamine transport or uptake for at least five biological half-lives. After each dose of iobenguane, wait at least 7 days before administering these medications.

Iobenguane Radiopharmaceutical Products

The therapeutic benefit of iobenguane radiopharmaceutical products may be reduced by CNS stimulants. Treatment: Before administering iobenguane, stop taking any medications that could impede or interfere with catecholamine transport or uptake for at least five biological half-lives. After each dose of iobenguane, wait at least 7 days before administering these medications.

Monoamine Oxidase Inhibitors

Amphetamines' ability to cause hypertension may be increased. However, unlike other monoamine oxidase inhibitors, linezolid and tedizolid have different management recommendations. For more information, consult the monographs for those agents. Linezolid and Tedizolid are exceptions.

Sibutramine

May intensify the harmful or hazardous effects of drugs that act centrally on weight loss.

Monitoring parameters:

  • Monitor weight every three months.
  • Monitor blood pressure.

How to administer Phentermine?

  • You should take it in the morning. Combining the drug with behavioral therapies and a low-calorie diet can result in significant weight loss.

Capsules and tablets (exclusion Lomaira)

  • Tablets and capsules shouldn't be consumed before breakfast or within one to two hours of breakfast on an empty stomach.
  • You can divide the tablets into two equal halves, and give two doses.

Tablet (Lomaira only):

  • It needs to be taken 30 minutes before meals.
  • The pills can be separated into two half since they are scored.

Orally disintegrating tablets (ODT):

  • Dry hands should be used to hold the tablets on the tongue while you wait for them to dissolve.
  • Then, it can be ingested either with or without water.
  • You can take the pills with or without food.

Mechanism of action of Phentermine (Adipex-P):

  • It is similar to amphetamines in pharmacological properties and acts as a sympathomimetic drug.It acts on the central nervous system to reduce appetite. 
  • It stimulates the hypothalamus, and releases norepinephrine.

Absorption:

  • It is easy to absorb.
  • The absorption of the supplement is affected if it is taken with meals and, especially, with high-fat meals.
  • Fasting conditions are not conducive to disintegrating tablets orally.

Protein binding:

  • 17.5%

Metabolism:

  • It is metabolized in the liver via p-hydroxylation (aromatic ring) and N-oxidation (alipthatic side chain).
  • It is not extensively metabolized, however, the main enzyme responsible for its metabolism is CYP3A4.

Half-life elimination:

  • About 20 hours

Time to peak:

  • 3 - 4.4 hours

Excretion:

  • It is excreted primarily in urine (62%-85% as unchanged drug)

International Brand Names of Phentermine:

  • Adipex-P
  • Lomaira
  • Suprenza
  • RHO-Phentermine
  • Acxion
  • Acxion AP
  • Adipex
  • Adipex Retard
  • Duromine
  • Furimin
  • Ionamin
  • Ionamine
  • Metermine
  • Mirapront
  • Mirubal
  • Normaform
  • Panbesy
  • Panbesy DCR
  • Pender
  • Phenkin
  • Razin
  • Redusa
  • Redusa Forte
  • Sinpet
  • Supremin
  • Terfamex
  • Vitupen
  • Weltmine

Phentermine Brand Names in Pakistan:

Phentermine Tablets 30 mg

Azura

Wilshire Laboratories (Pvt) Ltd.

Phentermine 30 mg Capsules

Azura

Wilshire Laboratories (Pvt) Ltd.