- Name of the medicinal product
Clomipramine Hydrochloride 75mg Tablets Taj Pharma
Clomipramine Hydrochloride 50mg Tablets Taj Pharma
Clomipramine Hydrochloride 25mg Tablets Taj Pharma
- Qualitative and quantitative composition
a) Each film coated Tablet Contains:
Clomipramine Hydrochloride BP 75mg
Colour: Ponceau 4R
b) Each film coated Tablet Contains:
Clomipramine Hydrochloride BP 50mg
Colour: Ponceau 4R
c) Each film coated Tablet Contains:
Clomipramine Hydrochloride BP 25mg
Colour: Ponceau 4R
For the full list of excipients, see section 6.1.
- Pharmaceutical form
- Clinical particulars
4.1 Therapeutic indications
Clomipramine Tablets are indicated for the treatment of:
– the symptoms of depressive illness especially where sedation is required
– obsessional and phobic states
– adjunctive treatment of cataplexy associated with narcolepsy.
Children and adolescents
In children and adolescents, there is not sufficient evidence of safety and efficacy of clomipramine in the treatment of depressive states, phobias and cataplexy associated with narcolepsy. The use of clomipramine in children and adolescents (0-17 years of age) in these indications is therefore not recommended (see section 4.4).
4.2 Posology and method of administration
Before initiating treatment with clomipramine, hypokalaemia should be treated (see section 4.4).
After a response has been obtained, maintenance therapy should be continued at the optimum dose to avoid relapse. Patients with a history of recurrence require maintenance treatment for a longer duration. Duration of maintenance treatment and need for further treatment should be reviewed periodically.
As a precaution against possible QTc prolongation and serotonergic toxicity, adherence to the recommended doses of clomipramine is advised and any increase in dose should be made with caution if drugs that prolong QT interval or other serotonergic agents are co-administered (see sections 4.4 and 4.5).
Abrupt discontinuation of clomipramine therapy should be avoided because of possible withdrawal symptoms. Therefore, dosage should be stopped gradually after regular use for long duration and the patient should be monitored carefully when clomipramine therapy is discontinued.
Oral – 75 mg/day initially, increasing gradually to 30-150 mg/day, if required, in divided doses throughout the day or as a single dose at bedtime. Many patients will be adequately maintained on 30-50 mg/day. Higher doses may be needed in some patients, particularly those suffering from obsessional or phobic disorders. In severe cases this dosage can be increased up to a maximum of 250 mg per day. Once a distinct improvement has set in, the daily dosage may be adjusted to a maintenance level of about 50-100 mg.
Elderly patients generally show a stronger response to clomipramine than patients of intermediate age groups, clomipramine should be used with caution in elderly patients and doses should be increased cautiously. The initial dose should be 10 mg/day, which may be increased with caution under close supervision to an optimum level of 30-75 mg daily which should be reached after about 10 days and then maintained until the end of treatment.
Not recommended (see section 4.4).
The maintenance dosage of clomipramine is generally higher than that used in depression. It is recommended that the dose be built up to 100-150 mg clomipramine daily, according to the severity of the condition. This should be attained gradually over a period of 2 weeks starting with 1 x 25 mg clomipramine daily. In elderly patients and those sensitive to tricyclic antidepressants a starting dose of 1 x 10 mg clomipramine daily is recommended. Again where a higher dosage is required the sustained-release 75 mg formulation may be preferable.
Adjunctive treatment of cataplexy associated with narcolepsy
(Oral treatment): 10-75 mg daily. It is suggested that treatment is commenced with 10 mg clomipramine daily and gradually increased until a satisfactory response occurs. Control of cataplexy should be achieved within 24 hours of reaching the optimal dose. Where necessary, therapy may be combined with Tablets up to the maximum dose of 75 mg per day.
Abrupt withdrawal should be avoided because of possible adverse reactions. If the decision is made to discontinue treatment, medication should be tapered, as rapidly as is feasible, but with recognition that abrupt discontinuation can be associated with certain symptoms (see sections 4.4 and 4.8 for a description of the risks of discontinuation of clomipramine).
Clomipramine should be given with caution in patients with renal impairment (see sections 4.4 and 5).
Clomipramine should be given with caution in patients with hepatic impairment (see sections 4.4 and 5).
Method of administration
For oral use
– hypersensitivity to the active substance or to any of the excipients listed in section 6.1 or cross-sensitivity to tricyclic antidepressants of the dibenzazepine group
– recent myocardial infarction, any degree of heart block or other cardiac arrhythmias
– severe liver disease
– concurrent administration with monoamine oxidase inhibitors or within 3 weeks of start or cessation of therapy (see section 4.5)
– concomitant treatment with selective, reversible MAO-A inhibitors, such as moclobemide
– narrow-angle glaucoma
– retention of urine
4.4 Special warnings and precautions for use
Suicide/suicidal thoughts or clinical worsening
Depression is associated with an increased risk of suicidal thoughts, self-harm and suicide (suicide-related events). This risk persists until significant remission occurs. As improvement may not occur during the first few weeks or more of treatment, patients should be closely monitored until such improvement occurs. It is general clinical experience that the risk of suicide may increase in the early stages of recovery.
Other psychiatric conditions for which clomipramine is prescribed can also be associated with an increased risk of suicide-related events. In addition, these conditions may be co-morbid with major depressive disorder. The same precautions observed when treating patients with major depressive disorder should therefore be observed when treating patients with other psychiatric disorders.
Patients with a history of suicide-related events, or those exhibiting a significant degree of suicidal ideation prior to commencement of treatment are known to be at greater risk of suicidal thoughts or suicide attempts, and should receive careful monitoring during treatment. A meta-analysis of placebo-controlled clinical trials of antidepressant drugs in adult patients with psychiatric disorders showed an increased risk of suicidal behaviour with antidepressants compared to placebo in patients less than 25 years old.
Close supervision of patients and in particular those at high risk should accompany drug therapy especially in early treatment and following dose changes. Patients (and caregivers of patients) should be alerted about the need to monitor for any clinical worsening, suicidal behaviour or thoughts and unusual changes in behaviour and to seek medical advice immediately if these symptoms present.
Patients with depressive disorders, both adult and paediatric, may experience worsening of depression and/or suicidality or other psychiatric symptoms, whether or not they are taking antidepressant medication.
Clomipramine should not be used in the treatment of depressive states, phobias and cataplexy associated with narcolepsy in children and adolescents under the age of 18 years (see section 4.1).
Antidepressants increase the risk of suicide-related behaviours (suicide attempt and suicidal thoughts), and hostility (predominately aggression, oppositional behaviour and anger) were more frequently observed in clinical trials among children and adolescents treated with antidepressants compared to those treated with placebo. If based on clinical need, a decision to treat is nevertheless taken, the patient should be carefully monitored for the appearance of suicidal symptoms. In addition, long term safety data in children and adolescents concerning growth, maturation and cognitive behavioural development are lacking.
Families and care givers of both paediatric and adult patients being treated with antidepressants for both psychiatric and non psychiatric indications, should be alerted about the need to monitor patients for the emergence of other psychiatric symptoms (see section 4.8), as well as the emergence of suicidality, and to report such symptoms immediately to health care providers.
Prescriptions for clomipramine should be written for the smallest quantity of Tablets consistent with good patient management, in order to reduce the risk of overdose.
Modifying the therapeutic regimen, including possibly discontinuing the medication, should be considered in these patients, especially if these changes are severe, abrupt in onset, or were not part of the patient’s presenting symptoms (see also treatment discontinuation in section 4.4).
Other psychiatric effects
Many patients with panic disorders experience intensified anxiety symptoms at the start of the treatment with antidepressants. This paradoxical initial increase in anxiety is most pronounced during the first few days of treatment and generally subsides within two weeks.
Activation of psychosis has occasionally been observed in patients with schizophrenia receiving tricyclic antidepressants.
Hypomanic or manic episodes have also been reported during a depressive phase in patients with cyclic affective disorders receiving treatment with a tricyclic antidepressant. In such cases it may be necessary to reduce the dosage of clomipramine or to withdraw it and administer an antipsychotic agent. After such episodes have subsided, low dose therapy with clomipramine may be resumed if required.
In predisposed patients, tricyclic antidepressants may provoke pharmacogenic (delirious) psychoses, particularly at night. These disappear within a few days of withdrawing the drug.
As improvement in depression may not occur for the first two to four weeks treatment, patients should be closely monitored during this period.
Elderly patients are particularly liable to experience adverse effects, especially agitation, confusion, and postural hypotension.
Cardiac and vascular disorders
Clomipramine should be administered with particular precaution in patients with cardiovascular disorders, especially those with cardiovascular insufficiency, conduction disorders, (e.g. atrioventricular block grades I to III), arrhythmias. Monitoring of cardiac function and the ECG is indicated in such patients.
There may be a risk of QTc prolongation and torsades de pointes, particularly at supra-therapeutic doses or supra-therapeutic plasma concentrations of clomipramine, as occur in the case of co- medication with selective serotonin reuptake inhibitors (SSRIs). Therefore, concomitant administration of drugs that can cause accumulation of clomipramine should be avoided. Equally, concomitant administration of drugs that can prolong the QTc interval should be avoided (see section 4.5). It is established that hypokalaemia is a risk-factor of QTc prolongation and torsades de pointes. Therefore, hypokalaemia should be treated before initiating treatment with clomipramine (see section 4.5).
Before initiating treatment it is advisable to check the patient’s blood pressure, because individuals with hypotension or a labile circulation may react to the drug with a fall in blood pressure.
Due to the risk of serotonergic toxicity, it is advisable to adhere to recommended doses. Serotonin syndrome, with symptoms such as hyperpyrexia, myoclonus, agitation, seizures, delirium and coma, can possibly occur when clomipramine is administered with serotonergic co-medications such as SSRIs, SNaRIs, tricyclic antidepressants or lithium. Therefore, concomitant administration of drugs that can cause accumulation of clomipramine should be avoided (see sections 4.2 and 4.5). For fluoxetine a washout period of two to three weeks is advised before and after treatment with fluoxetine.
Tricyclic antidepressants are known to lower the convulsion threshold and clomipramine should therefore, be used with extreme caution in patients with epilepsy and other predisposing factors, e.g. brain damage of varying aetiology, concomitant use of neuroleptics, withdrawal from alcohol or drugs with anticonvulsive properties (e.g. benzodiazepines). It appears that the occurrence of seizures is dose dependent. Therefore, the recommended total daily dose of clomipramine should not be exceeded.
Concomitant treatment of clomipramine and electroconvulsive therapy should only be resorted to under careful supervision.
Because of its anticholinergic properties, clomipramine should be used with caution in patients with a history of increased intra-ocular pressure, narrow-angle glaucoma, urinary retention or with symptoms of bladder neck obstruction, e.g. diseases of the prostate, such as prostatic hypertrophy.
Decreased lacrimation and accumulation of mucoid secretions due to the anticholinergic properties of tricyclic antidepressants may cause damage to the corneal epithelium in patients with contact lenses.
Specific treatment populations
Caution is called for when giving tricyclic antidepressants to patients with severe hepatic disease and tumours of the adrenal medulla (e.g. phaeochromocytoma, neuroblastoma), in whom they may provoke hypertensive crises.
Caution is advised in patients with hyperthyroidism or during concomitant treatment with thyroid preparations since aggravation of unwanted cardiac effects may occur.
It is advisable to monitor cardiac and hepatic function during long-term therapy with clomipramine. In patients with hepatic and renal disease, periodic monitoring of hepatic enzyme levels and renal function is recommended.
An increase in dental caries has been reported during long-term treatment with tricyclic antidepressants. Regular dental check-ups are therefore advisable during long-term treatment.
Caution is called for in patients with chronic constipation. Tricyclic antidepressants may cause paralytic ileus, particularly in the elderly and in bed-ridden patients.
In elderly patients, tricyclic antidepressants may provoke pharmacogenic (delirious) psychoses, particularly at night. These disappear within a few days of withdrawing the drug.
Monitoring of cardiac function and the ECG is indicated in elderly patients.
White blood cell count
Although changes in the white blood cell count have been reported with clomipramine only in isolated cases, periodic blood cell counts and monitoring for symptoms such as fever and sore throat are called for, particularly during the first few months of therapy. They are also recommended during prolonged therapy.
Anticoagulants / Non-steroidal anti-inflammatory drugs
Skin and mucous membrane bleeding has been reported with clomipramine. The product should be used with caution among patients that simultaneously use medicines that increase the risk of bleeding, for example anticoagulants, salicylic acid derivatives and non-steroidal anti-inflammatory drugs (NSAIDs). Care should be taken in patients with an increased tendency to bleed.
Anaesthetics given during tri/tetracyclic antidepressant therapy may increase the risk of arrhythmias and hypotension.
Before general or local anaesthesia, the anaesthetist should be aware that the patient has been receiving clomipramine and of the possible interactions (see section 4.5).
Abrupt withdrawal should be avoided because of possible adverse reactions. If the decision is made to discontinue treatment, medication should be tapered, as rapidly as is feasible, but with recognition that abrupt discontinuation can be associated with certain symptoms (see section 4.8 for a description of the risks of abrupt discontinuation of clomipramine).
Clomipramine Tablets contain lactose. Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.
Clomipramine contains Sunset yellow (E110). May cause allergic reactions.
4.5 Interaction with other medicinal products and other forms of interaction
Interactions resulting in a contraindication
Do not give clomipramine for at least 3 weeks after discontinuation of treatment with MAO inhibitors (there is a risk of severe symptoms consistent with Serotonin Syndrome such as hypertensive crisis, hyperpyrexia, myoclonus, agitation, seizures, delirium and coma). The same applies when giving a MAO inhibitor after previous treatment with clomipramine. In both instances the treatment should initially be given in small gradually increasing doses and its effects monitored. There is evidence to suggest that clomipramine may be given as little as 24 hours after a reversible MAO-A inhibitor such as moclobemide, but the 3-week wash-out period must be observed if the MAO-A inhibitor is used after clomipramine.
Interactions resulting in a concomitant use not recommended
Diuretics may lead to hypokalaemia, which increases the risk of QTc prolongation and torsades de pointes. Hypokalaemia should therefore be treated prior to administration of clomipramine (see sections 4.2 and 4.4).
Tricyclic antidepressants should not be employed in combination with antiarrhythmic agents of the quinidine type.
Selective serotonin reuptake inhibitors (SSRIs)
SSRIs which are inhibitors of CYP2D6, such as fluoxetine, paroxetine, or sertraline, and of others including CYP1A2 and CYP2C19 (e.g. fluvoxamine), may also increase plasma concentrations of clomipramine, with corresponding adverse effects. Steady-state serum levels of clomipramine increased ~4-fold by co-administration of fluvoxamine (N-desmethylclomipramine decreased ~2-fold). In addition, co-medication with SSRIs may lead to additive effects on the serotonergic system (see serotonergic agents) (see sections 4.2 and 4.4).
Serotonin Syndrome can possibly occur when clomipramine is administered with other serotonergic co-medications such as selective serotonin reuptake inhibitors (SSRIs), serotonin and noradrenergic reuptake inhibitors (SNaRIs), tricyclic antidepressants and lithium (see sections 4.2 and 4.4). For fluoxetine, a wash-out period of two to three weeks is advised before and after treatment with fluoxetine.
Interactions to be considered
Interactions resulting in increased effect of clomipramine
Oral antifungal, terbinafine
Co-administration of clomipramine with terbinafine, a strong inhibitor of CYP2D6, may result in increased exposure and accumulation of clomipramine and its N-demethylated metabolite. Therefore, dose adjustments of clomipramine may be necessary when co-administered with terbinafine.
Co-administration with the histamine2 (H2)-receptor antagonist, cimetidine (an inhibitor of several P450 enzymes, including CYP2D6 and CYP3A4), may increase plasma concentrations of tricyclic antidepressants, whose dosage should therefore be reduced.
No interaction between chronic oral contraceptive use (15 or 30 micrograms ethinylestradiol daily) and clomipramine (25 mg daily) has been documented. Oestrogens are not known to be inhibitors of CYP2D6, the major enzyme involved in clomipramine clearance and, therefore, no interaction is expected. Although, in a few cases with high dose oestrogen (50 micrograms daily) and the tricyclic antidepressant imipramine, increased side effects and therapeutic response were noted, it is unclear as to the relevance of these cases to clomipramine and lower dose oestrogen regimens. Monitoring therapeutic response of tricyclic antidepressants at high dose oestrogen regimens (50 micrograms daily) is recommended and dose adjustments may be necessary.
Co-medication of antipsychotic (e.g. phenothiazines) may result in increased plasma levels of tricyclic antidepressants, a lowered convulsion threshold, and seizures. Combination with thioridazine may produce severe cardiac arrhythmias.
This drug may also increase plasma concentrations of tricyclic antidepressants, whose dosage should therefore be reduced.
Concomitant administration of valproate with clomipramine may cause inhibition of CYP2C and/or UGT enzymes resulting in increased serum levels of clomipramine and desmethylclomipramine.
Grapefruit, grapefruit juice, or cranberry juice
Concomitant administration of Clomipramine with grapefruit, grapefruit juice, or cranberry juice may increase the plasma concentrations of clomipramine.
Interactions resulting in decreased effect of clomipramine
Rifampicin (CYP3A and CYP2C inducer), may decrease clomipramine concentrations as concomitant administration of drugs known to induce cytochrome P450 enzymes, particularly CYP3A4, CYP2C19 may accelerate the metabolism and decrease the efficacy of clomipramine.
Anticonvulsants (CYP3A and CYP2C inducer) e.g. barbiturates, carbamazepine, phenobarbital and phenytoin, may decrease clomipramine concentrations as concomitant administration of drugs known to induce cytochrome P450 enzymes, particularly CYP3A4, CYP2C19 may accelerate the metabolism and decrease the efficacy of clomipramine.
Known inducers of CYP1A2 (e.g. nicotine/components in cigarette smoke), decrease plasma concentrations of tricyclic drugs. In cigarette smokers, clomipramine steady-state plasma concentrations were decreased 2-fold compared to non-smokers (no change in N– desmethylclomipramine).
Colestipol and cholestyramine
Concomitant administration of ion exchange resins such as cholestyramine or colestipol may reduce the plasma levels of clomipramine. Staggering the dosage of clomipramine and resins, such that the drug is administered at least 2 h before or 4-6 h after the administration of resins, is recommended.
St. John’s wort
Concomitant administration of clomipramine with St. John’s wort during the treatment may decrease the plasma concentrations of clomipramine.
Interactions affecting other drugs
Tricyclic antidepressants may potentiate the effects of these drugs (e.g. phenothiazines, antiparkinsonian agents, antihistamines, atropine, biperiden) on the eye, central nervous system, bowel and bladder).
Clomipramine may diminish or abolish the antihypertensive effects of guanethidine, betanidine, reserpine, clonidine and alpha-methyldopa. Patients requiring co-medication for hypertension should therefore be given antihypertensives of a different type (e.g. vasodilators, or beta-blockers).
It would be advisable to review all antihypertensive therapy during treatment with tricyclic antidepressants.
Tricyclic antidepressants may potentiate the effects of alcohol and other central depressant substances (e.g. barbiturates, benzodiazepines, or general anaesthetics).
Clomipramine may potentiate the cardiovascular effects of adrenaline, ephedrine, isoprenaline, noradrenaline, phenylephrine, and phenylpropanolamine (e.g. as contained in local and general anaesthetic preparations and nasal decongestants).
Tricyclic antidepressants may potentiate the anticoagulant effect of coumarin drugs by inhibiting their metabolism by the liver. Careful monitoring of plasma prothrombin is therefore advised.
Drugs that can cause increase plasma clomipramine levels or which in themselves prolong the QTc interval
The risk of QTc prolongation and torsades de pointes is likely to be increased if clomipramine is co-administered with other drugs that can cause QTc prolongation. Therefore concomitant use of such agents with clomipramine is not recommended (see section 4.4). Examples include certain antiarrhythmics, such as those of Class 1A (such as quinidine, disopyramide and procainamide) and Class III (such as amiodarone and sotalol), tricyclic antidepressants (such as amitriptyline), certain tetracyclic antidepressants (such as maprotiline), certain antipsychotic medications (such as phenothiazines and pimozide), certain antihistamines (such as terfenadine); lithium, quinine and pentamidine. This list is not exhaustive. The risk of QTc prolongation and torsades de pointes is likely to be increased if clomipramine is co-administered with drugs that can cause increased plasma clomipramine levels. Clomipramine is metabolised by cytochrome P450 2D6 and the plasma concentration of clomipramine may therefore be increased by drugs that are either substrates and/or inhibitors of this P450 isoform. Therefore, concurrent use of these drugs with clomipramine is not recommended (see section 4.4). Examples of drugs which are substrates or inhibitors of cytochrome P450 2D6 include antiarrhythmics, certain antidepressants including SSRIs, tricyclic antidepressants and moclobemide; certain antipsychotics; β-blockers; protease inhibitors, opiates, ecstasy (MDMA), cimetidine and terbinafine. This list is not exhaustive.
Calcium channel blockers
Diltiazem and verapamil may increase the plasma concentration of imipramine, and possibly other tricyclics.
Non-steroidal anti-inflammatory drugs
The potential pharmacodynamic interactions with drugs that increase the risk of bleeding, for example, salicylic acid derivatives, non-steroidal anti-inflammatory / antirheumatic drugs (NSAIDs) should be considered because of the increased risk of bleeding with concomitant clomipramine.
Altretamine: risk of severe postural hypotension.
Possible increased side effects with nefopam; possible increased risk of convulsions with tramadol; possible increased sedation with opioid analgesics; increased risk of ventricular arrhythmias with levacetylmethadol.
Increased risk of ventricular arrhythmias – avoid concomitant use with pimozide. Antipsychotic agents may increase the plasma concentration of tricyclic agents. No such effects are known to occur in combination with diazepam, but it might be necessary to reduce the dosage of clomipramine if administered concomitantly with alprazolam or disulfiram. There may be increased antimuscarinic side-effects with phenothiazines, and possibly clozapine.
Concomitant use of tricyclic antidepressants and entacapone should be avoided; central nervous system toxicity has been reported with selegiline.
Tricyclic antidepressants may enhance the muscle relaxant effect of baclofen.
4.6 Fertility, pregnancy and lactation
Women of child-bearing potential
There are no data supporting any special recommendations in women of child-bearing potential.
There is limited amount of data from the use of clomipramine in pregnant women that indicates a potential to harm the foetus or cause congenital malformation.
Neonates whose mothers had taken tricyclic antidepressants up until delivery have developed dyspnoea, lethargy, colic, irritability, hypotension or hypertension, tremor or spasms, during the first few hours or days.
Studies in animals have shown reproductive toxicity (see section 5.3). Clomipramine is not recommended during pregnancy and in women of childbearing potential not using contraception.
Clomipramine passes into the breast milk in small quantities. Therefore nursing mothers should be advised to withdraw the medication or cease breast-feeding.
Clomipramine hydrochloride did not appear to have any significant effects on fertility and general reproductive performance.
4.7 Effects on ability to drive and use machines
Patients receiving clomipramine should be warned that blurred vision, drowsiness and other nervous system and psychiatric related disorders such as somnolence, disturbance in attention, confusion, disorientation, aggravation of depression, delirium etc (see section 4.8) have been observed. In the presence of such effects, patients should not drive, operate machinery or do anything else which may require alertness or quick actions. Patients should also be warned that alcohol or other drugs may potentiate these effects (see section 4.5).
This medicine can impair cognitive function and can affect a patient’s ability to drive safely. This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act 1988. When prescribing this medicine, patients should be told:
- The medicine is likely to affect your ability to drive
- Do not drive until you know how the medicine affects you
- It is an offence to drive while under the influence of this medicine
- However, you would not be committing an offence (called ‘statutory defence’) if:
o The medicine has been prescribed to treat a medical or dental problem and
o You have taken it according to the instructions given by the prescriber and in the information provided with the medicine and
o It was not affecting your ability to drive safely
4.8 Undesirable effects
Unwanted effects are usually mild and transient, disappearing under continued treatment or with a reduction in the dosage. They do not always correlate with plasma drug levels or dose. It is often difficult to distinguish certain undesirable effects from symptoms of depression such as fatigue, sleep disturbances, agitation, anxiety, constipation, and dry mouth.
If severe neurological or psychiatric reactions occur, clomipramine should be withdrawn.
Adverse reactions are ranked under heading of frequency, the most frequent first, using the following convention: very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to < 1/100); rare (≥1/10,000 to < 1/1,000); very rare (<1/10,000); not known (cannot be estimated from the available data).
|Blood and lymphatic system disorders|
|Very rare||Leucopenia, agranulocytosis, thrombocytopenia, eosinophilia|
|Immune system disorders|
|Very rare||Anaphylactic and anaphylactoid reactions including hypotension|
|Very rare||SIADH (inappropriate antidiuretic hormone secretion syndrome)|
|Metabolism and nutrition disorders|
|Very common||Increased appetite|
|Common||Confusional state, disorientation, hallucinations (particularly in elderly patients and patients with Parkinson’s disease), anxiety, agitation, sleep disorder, mania, hypomania, aggression, depersonalisation, aggravation of depression, insomnia, nightmares, delirium|
|Uncommon||Activation of psychotic symptoms|
|Not known||Suicidal ideation, suicidal behaviours2|
|Nervous system disorders|
|Very common||Dizziness, tremor, headache, myoclonus, somnolence|
|Common||Speech disorder, paraesthesia, hypertonia, dysgeusia, memory impairment, disturbance in attention|
|Very rare||Neuroleptic malignant syndrome1|
|Not known||Serotonin syndrome, extrapyramidal disorder (including akathisia and tardive dyskinesia)3|
|Very common||Accommodation disorder, vision blurred|
|Ear and labyrinth disorders|
|Common||Sinus tachycardia, palpitation, orthostatic hypotension, clinically irrelevant ECG changes (e.g. ST and T changes) in patients of normal cardiac status|
|Uncommon||Arrhythmias, blood pressure increased|
|Very rare||Conduction disorder (e.g. widening of QRS complex, prolonged QT interval, PQ changes, bundle-branch block, torsades de pointes, particularly in patients with hypokalaemia)|
|Respiratory, thoracic, and mediastinal disorders|
|Very rare||Alveolitis allergic (pneumonitis) with or without eosinophilia|
|Very common||Nausea, dry mouth, constipation|
|Common||Vomiting, gastrointestinal disorders, diarrhoea|
|Very rare||Hepatitis with or without jaundice|
|Skin and subcutaneous tissue disorders|
|Common||Dermatitis allergic (skin rash, urticaria), photosensitivity reaction, pruritus|
|Very rare||Ecchymosis, purpura, alopecia|
|Musculoskeletal and connective tissue disorders|
|Not known||Rhabdomyolysis (as a complication of neuroleptic malignant syndrome)3|
|Renal and urinary disorders|
|Very common||Micturition disorder|
|Reproductive system and breast disorders|
|Very common||Libido disorder, erectile dysfunction|
|Common||Galactorrhoea, breast enlargement, women occasionally experience orgasmic impotence|
|Not known||Ejaculation failure, ejaculation delayed|
|General disorders and administration site conditions|
|Very rare||Oedema (local or generalised), hyperpyrexia|
|Very common||Weight increased, blood sugar changes|
|Very rare||Electroencephalogram abnormal|
|Not known||Blood prolactin increased3|
1 In post-marketing experience very rarely malignant neuroleptic syndrome has been reported although a causal relationship has not been confirmed.
2 Cases of suicidal ideation and suicidal behaviours have been reported during clomipramine therapy or early after treatment discontinuation (see section 4.4).
3 These adverse events were reported in patients treated with clomipramine based on post marketing reports.
The following symptoms commonly occur after abrupt withdrawal or reduction of the dose: nausea, vomiting, abdominal pain, diarrhoea, insomnia, headache, nervousness and anxiety (see section 4.4).
Epidemiological studies, mainly conducted in patients 50 years of age and older, show an increased risk of bone fractures in patients receiving SSRIs and TCAs. The mechanism leading to this risk is unknown.
Elderly patients are particularly sensitive to anticholinergic, neurological, psychiatric, or cardiovascular effects. Their ability to metabolise and eliminate drugs may be reduced, leading to a risk of elevated plasma concentrations at therapeutic doses.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product.
The signs and symptoms of overdose with clomipramine are similar to those reported with other tricyclic antidepressants. Cardiac abnormalities and neurological disturbances are the main complications. In children accidental ingestion of any amount should be regarded as serious and potentially fatal.
Signs and symptoms
Symptoms generally appear within 4 hours of ingestion and reach maximum severity after 24 hours. Owing to delayed absorption (anticholinergic effect), long half-life, and enterohepatic recycling of the drug, the patient may be at risk for up to 4-6 days.
The following signs and symptoms may be seen:
Central nervous system:
Drowsiness, stupor, coma, ataxia, restlessness, agitation, enhanced reflexes, muscular rigidity, athetoid and choreoathetoid movements, convulsions, serotonin syndrome (e.g. hypertensive crisis, hyperpyrexia, myoclonus, delirium and coma).
Hypotension, tachycardia, QTc prolongation and arrhythmia including torsades de pointes, conduction disorders, shock, heart failure; in very rare cases cardiac arrest.
Respiratory depression, cyanosis, vomiting, fever, mydriasis, sweating and oliguria or anuria may also occur.
There is no specific antidote, and treatment is essentially symptomatic and supportive.
Anyone suspected of receiving an overdose of clomipramine, particularly children, should be hospitalised and kept under close surveillance for at least 72 hours.
Perform gastric lavage or induce vomiting as soon as possible if the patient is alert. If the patient has impaired consciousness, secure the airway with a cuffed endotracheal tube before beginning lavage, and do not induce vomiting. These measures are recommended for up to 12 hours or even longer after the overdose, since the anticholinergic effect of the drug may delay gastric emptying. Administration of activated charcoal may help to reduce drug absorption.
Treatment of symptoms is based on modern methods of intensive care, with continuous monitoring of cardiac function, blood gases, and electrolytes, and if necessary, emergency measures such as:
For respiratory failure:
– intubation and artificial respiration.
For cardiovascular symptoms:
– in severe hypotension the patient should be placed in an appropriate position and be given a plasma expander, dopamine, or dobutamine by intravenous drip.
– cardiac arrhythmias must be treated according to the requirements of the case.
– implantation of a cardiac pacemaker should be considered.
– low potassium values and acidosis should be corrected.
In all patients with ECG abnormalities, cardiac function should – even after the ECG tracings have reverted to normal – be kept under close observation for at least another 48 hours because relapses may occur.
Treatment of torsades de pointes:
If torsades de pointes should occur during treatment with clomipramine, the drug should be discontinued and hypoxia, electrolyte abnormalities and acid base disturbances should be corrected. Persistent torsades de pointes may be treated with magnesium sulphate 2 g (20 ml of 10% solution) intravenously over 30-120 seconds, repeated twice at intervals of 5-15 minutes if necessary. Alternatively, if these measures fail, the arrhythmia may be abolished by increasing the underlying heart rate. This can be achieved by atrial and ventricular pacing or by isoprenaline (isproterenol) infusion to achieve a heart rate of 90-110 beats per minute. Torsades de pointes is usually not helped by antiarrhythmic drugs and those which prolong the QTc interval (e.g. amiodarone, quinidine) may make it worse.
Since it has been reported that physostigmine may cause severe bradycardia, asystole and seizures, its use is not recommended in cases of overdosage with clomipramine. Haemodialysis or peritoneal dialysis are ineffective because of the low plasma concentrations of clomipramine.
Diazepam should be given iv or other anticonvulsants such as phenobarbitone or paraldehyde (these substances may exacerbate existing respiratory failure, hypotension, or coma).
- Pharmacological properties
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antidepressants, Non-selective monoamine reuptake inhibitors.
Mechanism of action
The therapeutic activity of clomipramine is believed to be based on its ability to inhibit the neuronal re-uptake of noradrenaline (NA) and serotonin (5-HT) released in the synaptic cleft, with inhibition of 5-HT reuptake being the more important of these activities.
Clomipramine also has a wide pharmacological spectrum of action, which includes alpha1- adrenolytic, anticholinergic, antihistaminic, and antiserotonergic (5-HT-receptor blocking) properties.
5.2 Pharmacokinetic properties
The active substance is completely absorbed following oral administration and intramuscular injection.
The systemic bioavailability of unchanged clomipramine is reduced by 50% by “first-pass” metabolism to desmethylclomipramine (an active metabolite). The bioavailability of clomipramine is not markedly affected by the ingestion of food but the onset of absorption and therefore the time to peak may be delayed. Coated tablets and sustained release tablets are bioequivalent with respect to amount absorbed.
During oral administration of constant daily doses of clomipramine the steady state plasma concentrations of clomipramine and desmethylclomipramine (active metabolite) and the ratio between these concentrations show a high variability between patients, e.g. 75 mg clomipramine daily produces steady state concentrations of clomipramine ranging from about 20 to 175 ng/ml. Levels of desmethylclomipramine follow a similar pattern but are 40-85% higher.
Clomipramine slows gastro-intestinal transit time, absorption can, however, be delayed, particularly in overdosage.
Clomipramine and desmethylclomipramine are widely distributed throughout the body and is 97.6% bound to plasma and tissue protein. The apparent volume of distribution is about 12-17 l/kg body weight. Concentrations in cerebrospinal fluid are about 2% of the plasma concentration.
It is reported to have a low and variable bioavailability following oral administration (48.2% of that after intravenous administration) and this has been related to extensive first-pass hepatic metabolism. Following single oral doses of 50 mg and 100 mg in healthy volunteers peak plasma concentrations of clomipramine of 28.8 ± 11.2 ng/ml range 16.5 to 53 ng/ml (at 3 to 5 hours post-dose) and 70-140 ng/ml (at 1 to 2.5 hours post-dose) respectively are reported). Peak plasma concentrations of desmethylclomipramine of 5.0 ± 1.4 ng/ml (range 2.9 to 7.8 ng/ml have been reported to occur between 5 to 12 hours after a single oral dose of 50 mg.
After chronic administration in depressed patients steady state plasma concentrations of clomipramine have been noted to vary 20 to 30 fold. Vandel et al reported that following repeated doses of 75 mg a day for 1 month, steady state plasma concentrations of clomipramine and desmethylclomipramine were 124.5 ± 94 ng/ml and 144.8 ± 113 ng/ml respectively.
The major route of transformation of clomipramine is demethylation to desmethylclomipramine. In addition, clomipramine and desmethylclomipramine are hydroxylated to 8-hydroxy-clomipramine and 8-hydroxy-desmethyl-clomipramine but little is known about their activity in vivo. The hydroxylation of clomipramine and desmethylclomipramine is under genetic control similar to that of debrisoquine. In poor metabolisers of debrisoquine this may lead to high concentrations of desmethylclomipramine; concentrations of clomipramine are less significantly influenced.
Oral clomipramine is eliminated from the blood with a mean half-life of 21 hours (range 12-36 h), and desmethylclomipramine with a half-life of 36 hours.
About two-thirds of a single dose of clomipramine is excreted in the form of water-soluble conjugates in the urine, and approximately one-third in the faeces. The quantity of unchanged clomipramine and desmethylclomipramine excreted in the urine amounts to about 2% and 0.5% of the administered dose respectively.
In the elderly, plasma clomipramine concentrations may be higher for a given dose than would be expected in younger patients because of reduced metabolic clearance.
Hepatic and renal impairment
The effects of hepatic and renal impairment on the pharmacokinetics of clomipramine have not been determined.
5.3 Preclinical safety data
Phospholipidosis and testicular changes considered to be secondary to the phospholipidosis, commonly associated with tricyclic compounds, have been observed with clomipramine hydrochloride at doses >4 fold greater than the maximum recommended human daily dose (MRHD). The clinical relevance of these findings is unknown.
Clomipramine hydrochloride demonstrated evidence of embryotoxicity e.g. increased embryolethality and growth retardation, in the rat and mouse studies (at doses which are 5 to 10 times the estimated oral MRHD of 5 mg/kg on a mg/kg basis), but not in the rabbit study. The safety margin for increased embryolethality based on the administered dose is 2.5 times the oral MHRD.
No teratogenic effects were detected in mice, rats, and rabbits at doses up to 100, 50, and 60 mg/kg, respectively.
Various in vitro and in vivo mutagenicity tests were performed and did not reveal any mutagenic activity of clomipramine hydrochloride.
The administration of clomipramine hydrochloride to mice and rats for 104 weeks did not show any evidence of carcinogenicity at dose levels representing 16 – 20 times the estimated oral MRHD of 5 mg/kg on a mg/kg basis.
- Pharmaceutical particulars
6.1 List of excipients
Eudragit, Calcium hydrogen phosphate, Silicon dioxide, Calcium stearate, Hypromellose, Red iron oxide, polyoxyl hydrogenated castor oil, talc and titanium dioxide.
6.3 Shelf life
6.4 Special precautions for storage
Do not store above 30°C
6.5 Nature and contents of container
Packs of 5, 10, 15, 20, 25, 30, 60, 90, 100, 120, and 180 Tablets in:
Aluminium foil/PVC blister packs
Not all pack sizes may be marketed.
6.6 Special precautions for disposal and other handling
7. Manufactured By:
Taj Pharmaceuticals Ltd. (Mumbai, India)
Unit No. 214, Old Bake House,
Maharashtra Chambers of commerce Lane,Fort,
Mumbai-400001 at: Ahmedabad- Gujarat, INDIA.
Clomipramine HCl 50mg Tablets Taj Pharma
Patient information leaflet
Read all of this information carefully before you start taking this medicine.
- Keep this leaflet. You may need to read it again.
- If you have further questions, ask your doctor or pharmacist.
- This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.
- If any of the side effects get serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
In this leaflet
- What Clomipramine HCl is and what it is used for
- Before you take Clomipramine HCl
- How to take Clomipramine HCl
- Possible side effects
- How to store Clomipramine HCl
- Further information
- What Clomipramine HCl is and what it is used for
Clomipramine HCl contains a medicine called clomipramine hydrochloride. This belongs to a group of medicines called “tricyclic antidepressants”. Clomipramine HCl is thought to work either by increasing the amount of chemical “messengers” in the brain or by making their effects last longer.
Clomipramine HCl is used to treat depression, obsessions and phobias (irrational fears). It is also used to treat muscular weakness (cataplexy) associated with repeat attacks of extreme sleepiness (narcolepsy) in adults.
- Before you take Clomipramine HCl
Do not take Clomipramine HCl if:
- you are allergic (hypersensitive) to clomipramine or any of the other ingredients of Clomipramine HCl (listed in Section6 below)
- you have ever had a rash or other allergic reaction to any other antidepressants
- you have had a heart attack within the last 3 months
- you have any serious heart disease
- you have any serious liver disease
- you have any other mental illness apart from depression, obsessions or phobias
- you have glaucoma (increased eye pressure)
- you have difficulty in passing urine
- you are pregnant, might become pregnant or are breast-feeding
- you are aged under 18
- you are taking medicines for depression called monoamine oxidase inhibitors (MAOIs), or have taken them within the last 3 weeks.
Do not take Clomipramine HCl if any of the above apply to you. If you are not sure, talk to your doctor or pharmacist before taking Clomipramine HCl.
Take special care with Clomipramine HCl
Check with your doctor or pharmacist before taking your medicine if:
- you have epilepsy (fits)
- you have an overactive thyroid gland
- you have a tumour (cancer) of the adrenal gland (such as phaeochromocytoma or neuroblastoma)
- you have low blood pressure
- you wear contact lenses
- you have had severe constipation for a long time
- you find yourself thinking about suicide
- you have had a head injury and suffered brain damage
- you are going to have ECT (electroconvulsive therapy)
- you have an irregular heart beat or other problems with your heart
- you have been diagnosed as having a low level of potassium in your blood (hypokalemia)
you have schizophrenia or any other mental disorder
- you are elderly
- you have glaucoma (increased pressure in the eye)
- you have liver or kidney disease
- you have any blood disorder
- you have difficulties in passing urine (e.g. due to diseases of the prostate)
- you easily faint
If any of the above apply to you (or you are not sure), talk to your doctor or pharmacist before taking Clomipramine HCl.
Taking other medicines
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines. This includes medicines obtained without a prescription, including herbal medicines. Clomipramine HCl interacts with a large number of medicines.
In particular, do not take Clomipramine HCl if you are taking the following:
- medicines for depression called monoamine oxidase inhibitors (MAOIs), or have taken them within the last 3 weeks.
Do not take Clomipramine HCl if this applies to you. If you are not sure, talk to your doctor or pharmacist before taking Clomipramine HCl.
Tell your doctor if you are taking any of the following:
- other medicines for depression called SSRIs e.g. fluoxetine, fluvoxamine; tricyclic antidepressants
e.g. barbiturates, benzodiazepines
- medicines for other mental illnesses such as schizophrenia or manic depression e.g. thioridazine, lithium
- medicines for high blood pressure
- medicines to treat heart disorders, particularly those used to treat an abnormal heart rhythm
- anticoagulants (blood thinning tablets like warfarin)
- medicines for Parkinson’s Disease
- drugs which affect the liver (your doctor will know which these are). They include nicotine and barbiturates
- cold, flu or hayfever drugs such as antihistamines and decongestants
- carbamazepine or phenytoin (for epilepsy)
- cimetidine (for stomach problems)
- methylphenidate (Ritalin) prescribed for children with ADHD
- atropine or similar medicines (including eye drops)
- estrogens (e.g. contraceptive pill or hormone replacement therapy)
- a medicine called terbinafine (used orally to treat skin, hair or nail infections due to fungus)
- drugs used to reduce fat in blood
- grapefruit/grapefruit juice, cranberry juice
If any of the above apply to you (or you are not sure), talk to your doctor or pharmacist before taking Clomipramine HCl.
Operations, tests and check-ups
- Tell your doctor or dentist if you are planning to have an operation of any kind, as Clomipramine HCl may interact with local or general anaesthetic.
- Your doctor may want to do blood tests and check your heart and liver function while you are taking Clomipramine HCl.
- You should go to the dentist regularly if you take Clomipramine HCl for a long time. Clomipramine HCl can cause a dry mouth which may increase the chance of tooth decay.
Taking Clomipramine HCl with food and alcohol
- You should not drink alcohol during your treatment with Clomipramine HCl – it may affect you more than usual.
- You can take Clomipramine HCl with or without food
Pregnancy and breast-feeding
Do not take Clomipramine HCl if you are pregnant or might become pregnant. Do not take Clomipramine HCl if you are breast-feeding.
Ask your doctor or pharmacist for advice before taking any medicine, if you are pregnant, might become pregnant or are breast-feeding.
Driving and using machines
If you feel dizzy, tired or have blurred vision when you start to take Clomipramine HCl, do not drive or work with machinery until this effect has worn off.
Important information about some of the ingredients of Clomipramine HCl
Clomipramine HCl tablets contain polyoxyl hydrogenated castor oil which may cause stomach upset and diarrhoea.
Information for you, your family and caregivers
Information for you
If you are depressed or have anxiety disorders you can sometimes have thoughts of harming or killing yourself. These may be increased when you first start taking antidepressants, since these medicines all take time to
work, usually about two weeks but sometimes longer.
You may be more likely to have these thoughts if:
- if you have previously had thoughts about killing or harming yourself
- if you are a young adult. Information from clinical trials has shown an increased risk of suicidal behaviour in adults aged less than 25 years with psychiatric conditions who were treated with an antidepressant.
If you have thought of harming or killing yourself at any time, contact your doctor or go to a hospital straight away. You may find it helpful to tell a relative or close friend that you are depressed or have an anxiety disorder,
and ask them to read this leaflet. You might ask them to tell you if they think your depression or anxiety is getting worse, or if they are worried about changes in your behaviour.
Information for your family and caregivers
The patient should be monitored to see if they show signs of behavioural changes such as unusual anxiety, restlessness, sleeping problems, irritability, aggressiveness, over-excitedness or other unusual changes in behaviour, worsening of depression or thinking about suicide. Any such symptoms should be reported to the patient’s doctor, especially if they are severe, start suddenly or were not part of the patient’s presenting symptoms before. You should evaluate the emergence of such symptoms on a day to day basis,
especially early during anti-depressant treatment and when the dose is increased or decreased, since changes may be abrupt.
Symptoms such as these may be associated with an increased risk of suicidal thinking or behaviour and indicate a need for very close monitoring and possible changes in medication.
- How to take Clomipramine HCl
The doctor will tell you how much Clomipramine HCl to take and when to take it. Always follow the doctor’s instructions carefully. The dose will be on the pharmacist’s label. Check the label carefully. If you are not sure, ask your doctor or pharmacist.
Taking this medicine
- Swallow your Clomipramine HCl Tablets whole with a drink of water.
- Keep taking your medicine until your doctor tells you to stop. Do not stop because you do not feel any better.
This medicine may take up to 4 weeks to work.
- The medicine may be taken as one dose at night or as two separate doses during the day.
- For depression: 1 to 2 tablets daily. Severe cases may need even higher doses.
- For obsessions and phobias: 1 to 2 tablets daily.
- For cataplexy: 1 tablet daily.
If you are not sure how much Clomipramine HCl to take, ask your doctor or pharmacist.
Elderly patients often need a lower dose because they are more likely to experience side effects.
Your doctor will tell you about this.
If you take more Clomipramine HCl than you should
If you or anyone else, accidently takes too much Clomipramine HCl, tell your doctor or go to your nearest hospital casualty
department immediately. Take your medicine pack with you so that people can see what you have taken.
If you forget to take Clomipramine HCl
If you miss a dose, take the next dose at the usual time. Then go on as before. DO NOT take a double dose.
If you stop taking Clomipramine HCl
Do not stop taking Clomipramine HCl suddenly because this may cause withdrawal side effects. If the decision is made by your doctor to discontinue treatment, the dose you will receive will be cut down gradually to prevent the development of withdrawal symptoms. You may get these side effects if you stop taking Clomipramine HCl suddenly: feeling or being sick, stomach ache, diarrhoea, headache, difficulty sleeping, nervousness or anxiety. If you have any further questions on the use of this product, ask your doctor or pharmacist.
- Possible side effects
Like all medicines, Clomipramine HCl can cause side effects. The side effects are usually mild and disappear as treatment continues.
Some side effects can be serious.
Stop taking Clomipramine HCl and tell your doctor immediately if you notice the following very rare symptoms:
- Rash, changes in blood pressure, swelling and increased fluid in tissues, and increased heart rate, difficulty with breathing and collapse. These may be signs of an allergic reaction.
- A high temperature and sweating with rigid muscles and confusion or agitation, or if you experience jerky
muscle movements which you can’t control. These may be signs of a serious condition known as neuroleptic malignant syndrome.
The side effects listed below have also been reported:
Very common (More than 1 in 10 people have experienced):
Increase in appetite and weight gain.
Headaches, dizziness, nausea, constipation, dry mouth, increased sweating, shaking hands, tremor, difficulty in passing urine, problems with their eyes, feeling tired or sleepy, sexual disturbances, restlessness.
Common (Up to 1 in 10 people have experienced):
Loss of appetite, stomach upset, vomiting, diarrhoea, light headedness when standing up (due to low blood pressure), increased anxiety, agitation, hot flushes, enlarged pupils, speech disturbances, yawning, feeling confused, disorientated or over excited, sleep disturbances, nightmares, hallucinations or thought disturbances, worsening of existing depression, impaired memory and concentration, aggressiveness, disturbances in heart rhythm, increased sensitivity of the skin to sunlight, rash and itching, breast changes, numbness or tingling in the arms and legs, muscle weakness, movement disorder, changes in liver function tests, taste disturbances, tinnitus (ringing in the ears), swelling of the breasts and discharge of milk, irritability, feeling detached from a situation (like watching it from afar).
Uncommon (Up to 1 in 100 people have experienced):
Mood changes including aggression, fits, movement disorders, increased blood pressure, irregular heart
Very rare (Up to 1 in 10,000 people have experienced):
Glaucoma, hepatitis causing jaundice (yellowing of the skin or whites of the eyes), and light coloured urine, urinary retention, oedema (generalised swelling), hair loss, blood disorders (which might result in persistent sore throat, fever or frequent infections, unexplained bruising or bruising more easily).
Most of the side effects are mild and may wear off after a few days treatment. If they are severe or
last more than a few days, tell your doctor. Also, if your medicine upsets you in any other way, tell your doctor.
Patients aged 50 years or older and taking a medicine of this group are more likely to experience bone fractures.
Children and Adolescents
Clomipramine HCl should not be used in the treatment of depressive states, phobias or cataplexy associated with narcolepsy in children and adults under the age of 18 years as long-term safety effects concerning growth, maturation and cognitive and behavioural development of Clomipramine HCl in this age group have not yet been demonstrated.
Also patients under 18 may have an increased risk of side effects such as suicidal thoughts, harming themselves and hostility (predominantly aggression, oppositional behaviours and anger) when they take drugs like Clomipramine HCl. Despite this, your doctor may prescribe Clomipramine HCl for patients under 18 because they decide that this is in their best interests. If your doctor has prescribed Clomipramine HCl for you (or your child) and you want to discuss this, please go back to your doctor.
You should inform your doctor if any of the symptoms listed above develop or worsen when patients under 18 are taking Clomipramine HCl.
Also reported (frequency not known)
Feeling of inner restlessness and a compelling need to be in constant motion, repetitive, involuntary, purposeless movements, breakdown of muscle, increase in prolactin (a hormone) level in the blood, and serotonin syndrome (syndrome caused due to increase in naturally occurring messenger, serotonin, in brain; manifested by symptoms like agitation, confusion, diarrhoea, high temperature, increased blood pressure, excessive sweating and rapid heartbeat), delayed or no ejaculation of semen if you are a male.
Reporting of side effects
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet.
- How to store Clomipramine HCl
Keep out of the reach and sight of children.
Do not use Clomipramine HCl after the expiry date, which is stated on the label and carton after EXP.
The expiry date refers to the last day of that month. Do not store above 30°C. Store in the original package in order to protect from moisture.
If your doctor tells you to stop taking Clomipramine HCl, please take any unused medicine back to your pharmacist to be destroyed. Do not throw it away with your normal household water or waste. This will help to protect the environment.
- Further information What Clomipramine HCl contains
- The active substance is clomipramine hydrochloride.
Each film-coated tablet contains 75mg /
Each film-coated tablet contains 50mg /
Each film-coated tablet contains 25mg
- The other ingredients are eudragit, calcium hydrogen phosphate, silicon dioxide, calcium stearate, hypromellose, red iron oxide, polyoxyl hydrogenated castor oil, talc and titanium dioxide.
What Clomipramine HCl looks like and the contents of the pack
Clomipramine HCl 75 mg Tablets are film-coated.
Clomipramine HCl 50 mg Tablets are film-coated.
Clomipramine HCl 30 mg Tablets are film-coated.
Packs of 5, 10, 15, 20, 25, 30, 60, 90, 100, 120, and 500Tablets in:
Aluminium foil/PVC blister packs
Not all pack sizes may be marketed.
7. Manufactured By:
Taj Pharmaceuticals Ltd. (Mumbai, India)
Unit No. 214, Old Bake House,
Maharashtra Chambers of commerce Lane,Fort,
Mumbai-400001 at: Ahmedabad- Gujarat, INDIA.
PIL: Patient Information Leaflet
SmPC: Summary of product characteristics
The Summary of Product Characteristics (or SmPC) of Clomipramine HCl Tablets is the most important regulatory document on a medicinal product because it is part of the marketing authorisation of a medicinal product and represents the basis of information for healthcare professionals on how to use the medicinal product safely and effectively.