Lofepramine
Lofepramine, sold under the brand names Gamanil, Lomont, and Tymelyt among others, is a tricyclic antidepressant which is used to treat depression. The TCAs are so named as they share the common property of having three rings in their chemical structure. Like most TCAs lofepramine is believed to work in relieving depression by increasing concentrations of the neurotransmitters norepinephrine and serotonin in the synapse, by inhibiting their reuptake. It is usually considered a third-generation TCA, as unlike the first- and second-generation TCAs it is relatively safe in overdose and has milder and less frequent side effects.
Lofepramine is not available in the United States, Canada, Australia or New Zealand, although it is available in Ireland, Japan, South Africa and the United Kingdom, among other countries.
Medical uses
In the United Kingdom, lofepramine is licensed for the treatment of depression which is its primary use in medicine.Contraindications
To be used with caution, or not at all, for people with the following conditions:- Heart disease
- Impaired kidney or liver function
- Narrow angle glaucoma
- In the immediate recovery period after myocardial infarction
- In arrhythmias
- Mania
- In severe liver and/or severe renal impairment
Pregnancy and lactation
Lofepramine use during pregnancy is advised against unless the benefits clearly outweigh the risks. This is because its safety during pregnancy has not been established and animal studies have shown some potential for harm if used during pregnancy. If used during the third trimester of pregnancy it can cause insufficient breathing to meet oxygen requirements, agitation and withdrawal symptoms in the infant. Likewise its use by breastfeeding women is advised against, except when the benefits clearly outweigh the risks, due to the fact it is excreted in the breast milk and may therefore adversely affect the infant. Although the amount secreted in breast milk is likely too small to be harmful.Side effects
The most common adverse effects include agitation, anxiety, confusion, dizziness, irritability, abnormal sensations, like pins and needles, without a physical cause, sleep disturbances and a drop in blood pressure upon standing up. Less frequent side effects include movement disorders, precipitation of angle closure glaucoma and the potentially fatal side effects paralytic ileus and neuroleptic malignant syndrome.Side effects with unknown frequency include :
- Digestive effects:
- * Constipation
- * Diarrhoea
- * Dry mouth
- * Nausea
- * Taste disturbances
- * Vomiting
- Effects on the heart:
- * Arrhythmia
- * ECG changes
- * Abnormal heart rhythm
- * Heart block
- * Sudden cardiac death
- * High heart rate
- Blood abnormalities:
- * Abnormal blood cell counts
- * Blood sugar changes
- * Low blood sodium levels
- Breast effects:
- * Breast enlargement, including in males.
- * Spontaneous breast milk secretion that is unrelated to breastfeeding or pregnancy
- Effects on the skin:
- * Abnormal sweating
- * Hair loss
- * Hives
- * Increased light sensitivity
- * Itching
- * Rash
- Mental / neurologic effects:
- * Delusions
- * Hallucinations
- * Headache
- * Hypomania/mania
- * Seizures
- * Suicidal behaviour
- Other effects:
- * Appetite changes
- * Blurred vision
- * Difficulty emptying the bladder
- * Difficulty talking due to difficulties in moving the required muscles
- * Liver problems
- * Ringing in the ears
- * Sexual dysfunction, such as impotence
- * Swelling
- * Weight changes
Withdrawal
Overdose
Compared to other TCAs, lofepramine is considered to be less toxic in overdose. Its treatment is mostly a matter of trying to reduce absorption of the drug, if possible, using gastric lavage and monitoring for adverse effects on the heart.Interactions
Lofepramine is known to interact with:- Alcohol. Increased sedative effect.
- Altretamine. Risk of severe drop in blood pressure upon standing.
- Analgesics. Increased risk of ventricular arrhythmias.
- Anticoagulants. Lofepramine may inhibit the metabolism of certain anticoagulants leading to a potentially increased risk of bleeding.
- Anticonvulsants. Possibly reduce the anticonvulsant effect of antiepileptics by lowering the seizure threshold.
- Antihistamines. Possible increase of antimuscarinic and sedative effects.
- Antimuscarinics. Possible increase of antimuscarinic side-effects.
- Anxiolytics and hypnotics. Increased sedative effect.
- Apraclonidine. Avoidance advised by manufacturer of apraclonidine.
- Brimonidine. Avoidance advised by manufacturer of brimonidine.
- Clonidine. Lofepramine may reduce the antihypertensive effects of clonidine.
- Diazoxide. Enhanced hypotensive effect.
- Digoxin. May increase risk of irregular heart rate.
- Disulfiram. May require a reduction of lofepramine dose.
- Diuretics. Increased risk of reduced blood pressure on standing.
- Cimetidine, diltiazem, verapamil. May increase concentration of lofepramine in the blood plasma.
- Hydralazine. Enhanced hypotensive effect.
- Monoamine oxidase inhibitors. Advised not to be started until at least 2 weeks after stopping MAOIs. MAOIs are advised not to be started until at least 1–2 weeks after stopping TCAs like lofepramine.
- Moclobemide. Moclobemide is advised not to be started until at least one week after treatment with TCAs is discontinued.
- Nitrates. Could possibly reduce the effects of sublingual tablets of nitrates.
- Rifampicin. May accelerate lofepramine metabolism thereby decreasing plasma concentrations of lofepramine.
- Ritonavir. May increase lofepramine concentration in the blood plasma.
- Sodium nitroprusside. Enhanced hypotensive effect.
- Thyroid hormones. Effects on the heart of lofepramine may be exacerbated.
Pharmacology
Pharmacodynamics
Lofepramine is a strong inhibitor of norepinephrine reuptake and a moderate inhibitor of serotonin reuptake. It is a weak-intermediate level antagonist of the muscarinic acetylcholine receptors.Lofepramine has been said to be a prodrug of desipramine, although there is also evidence against this notion.