Colchicine
Treatment for acute gout attacks and for chronic gout, prophylaxis of acute attacks at the start of treatment with uric acid mobilisers and periodic disease (familial Mediterranean fever).
MORE INFORMATION:
1 - NAME OF THE MEDICINAL PRODUCT.
COLCHICINE SEID 1 mg tablets
2 - QUALITATIVE AND QUANTITATIVE COMPOSITION.
Each tablet contains:
Colchicine………………………1.0 mg
Excipients: lactose ………… 61.5 mg
Methylene casein….. 3.0 mg
For the full list of excipients see section 6.1.
3 - PHARMACEUTICAL FORM.
Pink tablets.
4 - CLINICAL PARTICULARS
4.1 Therapeutic indications
Treatment for acute gout attacks and for chronic gout, prophylaxis of acute attacks at the start of treatment with uric acid mobilisers and periodic disease (familial Mediterranean fever).
4.2 Posology and method of administration
Colchicine has a narrow therapeutic index and is extremely toxic in case of overdose. The following dose should not be exceeded under any circumstances, as it could be fatal.
Oral administration.
The recommended dose depends on the patient’s age, renal and hepatic function and the concomitant use of other medications (see sections 4.4 and 4.5)
Adults.
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- Acute gout attack:
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The recommended dose is 1 tablet (1 mg) at the first sign of acute attack. If pain relief is not achieved, a second tablet (1 mg) can be administered one or two hours after the first dose. Do not administer doses of more than 2 mg in 24 hours. Doses higher than 2 mg a day have not shown greater efficacy, but the adverse effects are increased.
This dosing regimen can be administered for up to a maximum of 4 consecutive days, with a total cumulative dose of 6 mg in 4 days. If necessary because the pain of the gout attack persists, the above-described regimen may be repeated, but always after a “wash-out period” of least 3 days without treatment.
Preventive treatment of gout attacks during initial therapy with allopurinol or
uricosuric agents:
The recommended dose as preventive treatment of gout attacks is 1 mg daily.
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- Periodic disease or familial Mediterranean fever:
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The recommended dose is 1 to 2 mg daily. It may be administered in two daily doses or one single dose.
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- Treatment of chronic gout:
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The recommended dose as treatment of chronic gout is 1 mg daily.
Children and adolescents under 18 years of age.
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- Acute gout attack, prevention of gout attacks and chronic gout:
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There are insufficient data to make recommendations for this age group.
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- Periodic disease or familial Mediterranean fever:
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The recommended dose in children over 12 years is 1 mg to 2 mg daily. It may be administered in two daily doses or one single dose.
In children under 12 years, adequate dosing is not possible with this presentation of the medicinal product, but the approximate dose in children aged 4 to 6 years is 0.3 mg to 1.8 mg daily and in children aged 6 to 12 years, 0.9 mg to 1.8 mg daily. These doses may be administered in one or two doses.
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- Renal impairment.
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In patients with mild renal impairment (CrCl 50-80 ml/min), no dose adjustment is required (see sections 4.4 and 5.2), although close monitoring for possible adverse effects is recommended. If adverse effects do occur, it may be necessary to reduce the dose.
In patients with moderate renal impairment (CrCl 30-50 ml/min), it may be necessary to halve the dose and/or increase the intervals between doses.
In cases of severe renal impairment (CrCl < 30 ml/min), the use of colchicine is contraindicated (see section 4.3).
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- Hepatic impairment.
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In patients with mild to moderate hepatic impairment, no dose adjustment is required (see sections 4.4 and 5.2), although close monitoring for possible adverse effects is recommended. If adverse effects do occur, it may be necessary to reduce the dose.
In patients with severe hepatic impairment, a dose reduction is necessary, but this is not possible due to the presentation of this medicinal product; therefore, the use of Colchicine is contraindicated (see section 4.3).
Elderly patients and special populations.
In elderly patients or those with renal or hepatic impairment, alternative therapies should be used. If colchicine is to be administered to these patients, the cumulative dose over a 4-day period must not exceed 3 mg, instead of the recommended adult dose of 6 mg (see section 4.2).
4.3 Contraindications
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- Hypersensitivity to the active substance or to any of the excipients of this medicinal product.
- Pregnancy.
- Severe renal impairment and haemodialysis patients.
- Severe hepatic impairment.
- Severe gastrointestinal disorders.
- Stomach ulcer.
- Cardiac disorders.
- Haematological alterations, such as blood dyscrasias.
- For 14 days after using CYP3A4 and/or P-glycoprotein inhibitors.
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4.4. Special warnings and precautions for use
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- If diarrhoea occurs, discontinue the medication or reduce the dose.
- In elderly patients, children and debilitated or alcoholic patients, treatment with colchicine should be closely monitored because of the increased risk of cumulative toxicity in these populations.
- Leukopenia, granulocytopenia, thrombocytopenia, pancytopenia, aplastic anaemia and myelosuppression have been associated with the use of colchicine at therapeutic doses, so it is recommended that the patient should be monitored for side effects and have regular blood tests.
- In patients with hepatobiliary and renal dysfunction, it may be necessary to adjust the dose. During treatment of the acute gout attack, the patient should be continuously monitored in case of renal or hepatobiliary dysfunction.
- Colchicine is significantly excreted in the urine in healthy individuals. Colchicine clearance is decreased in patients with renal impairment. Total body clearance of colchicine is reduced by up to 75% in patients with kidney disease undergoing dialysis (see section 5.2).
- Colchicine cannot be eliminated in patients undergoing dialysis so, a priori, its use is contraindicated (see section 4.3).
- In patients with hepatic impairment, colchicine clearance may be significantly reduced and its plasma half-life increased.
- Neuromuscular toxicity and rhabdomyolysis have been reported with chronic treatment at therapeutic doses. This risk may be increased in patients with renal impairment and in elderly patients (even those without renal and hepatic impairment).
- Concomitant use of atorvastatin, simvastatin, pravastatin, fluvastatin, gemfibrozil, fenofibrate, fenofibric acid or bezafibrate (which themselves are associated with myotoxicity), digoxin or ciclosporin with colchicine may increase the occurrence of myopathies (see section 4.5). Once colchicine treatment is
discontinued, the symptoms usually disappear within a period of one week to several months.
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Warnings about excipients.
This medicinal product contains lactose. Patients with a hereditary galactose intolerance, Lapp lactase deficiency (deficiency observed in some towns in Lapland) or glucose-galactose malabsorption should not take this medicinal product.
This medicinal product contains methylene casein. Patients who are allergic or intolerant to cow’s milk protein
should not take this medicinal product.
4.5. Interaction with other medicinal products and other forms of interaction
Greater precaution should be taken when colchicine is combined with active substances that are metabolised by or interact with the cytochrome P450 system, in particular with the CYP3A4 isoenzyme or P-glycoprotein.
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- Anti-infective agents: colchicine toxicity is increased by simultaneous treatment with clarithromycin, erythromycin or telithromycin and CYP3A4 substrates and inhibitors, particularly in patients with pre-existing renal impairment. Other CYP3A4 inhibitors, such as itraconazole,
ketoconazole, indinavir, nelfinavir, ritonavir and saquinavir, may increase colchicine toxicity. - Calcium channel blockers: verapamil and diltiazem.
- Ciclosporin: colchicine should be used with caution in combination with ciclosporin due to the possible risk of increased neurotoxicity and myotoxicity.
- –Vitamins: the absorption of Vitamin B12 may be altered by chronic or high-dose administration of colchicine. Vitamin requirements may be increased.
- Anti-infective agents: colchicine toxicity is increased by simultaneous treatment with clarithromycin, erythromycin or telithromycin and CYP3A4 substrates and inhibitors, particularly in patients with pre-existing renal impairment. Other CYP3A4 inhibitors, such as itraconazole,
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Concomitant use of atorvastatin, simvastatin, pravastatin, fluvastatin, gemfibrozil, fenofibrate, fenofibric acid or bezafibrate (which themselves are associated with myotoxicity) may increase the occurrence of myopathies. Once treatment with colchicine is discontinued, the symptoms usually disappear within a period of one week to several months.
Ingestion of grapefruit juice (which inhibits CYP3A4) should be avoided during treatment with colchicine, as it may increase the toxicity of colchicine.
4.6. Fertility, pregnancy and lactation
Fertility
There are no data regarding the possible effects of colchicine on fertility.
Pregnancy
No malformations or foetal/neonatal toxicity were observed after colchicine exposure in a limited number of pregnant women with familial Mediterranean fever. However, animal studies with colchicine have shown teratogenic effects. Therefore, as a precautionary measure due to the absence of controlled studies in humans and because it crosses the placenta, with the consequent risk to the foetus due to its mechanism of action, its use during pregnancy is contraindicated (see sections 4.3 and 5.3)
Breast-feeding
Colchicine is excreted in human milk.
Colchicine should not be used during breast-feeding.
4.7 Effects on ability to drive and use machines
This medicine has not been reported to have any effect on the ability to drive and use machines.
4.8. Undesirable effects
Common adverse reactions that have been reported include nausea, vomiting and abdominal pain.
High doses may cause severe diarrhoea, gastrointestinal bleeding, skin rashes and hepatic or renal impairment.
Peripheral neuropathy, myopathy, rhabdomyolysis, alopecia and azoospermia have occurred occasionally, and with prolonged treatment there can be bone marrow failure with agranulocytosis, thrombocytopenia and aplastic anaemia.
Treatment should be discontinued and the patient should go to an emergency department at the first symptom of nausea, vomiting, abdominal pain or diarrhoea.
According to the AGREE study (see section 5.1), in which 185 patients with acute gout attack were allocated to three different treatment groups: high-dose colchicine treatment [1.2 mg followed by 0.6 mg every hour for 6 hours (total: 4.8 mg)], low-dose treatment [1.2 mg
followed by 0.6 mg in the next hour (total: 1.8 mg)] and placebo treatment, the incidence of adverse reactions in the different groups was 76.9%, 36.5% and 27.1%, respectively. The incidence of the most frequently reported adverse reactions is detailed below. See Vademecum
4.9 Overdose
Colchicine has a narrow therapeutic index and is extremely toxic in case of overdose. High-risk patients are those with hepatic or renal impairment, gastrointestinal or cardiac disorders and elderly patients.
Because colchicine overdose is complex, specialist advice should be obtained rapidly to manage the overdose as promptly as possible.
The exact dose of colchicine that causes significant toxicity is unknown. Deaths have been reported after ingestion of doses as low as 7 mg over a 4-day period, while there are cases of patients who survived taking doses of more than 60 mg.
From a review of 150 overdose patients, it has been established that those who ingested a dose lower than 0.5 mg/kg survived, with a milder toxicity profile, while subjects who took doses between 0.5 and 0.8 mg/kg experienced more severe reactions, including myelosuppression. There was a 100% mortality rate in subjects who ingested more than 0.8 mg/kg.
There may be a delay of up to 6 hours before toxicity becomes apparent and some signs may even be delayed for up to a week or more. Therefore, any patient with suspected overdose, even without apparent signs, should seek specialist medical attention immediately.
The first signs of acute colchicine toxicity usually appear approximately 24 hours after ingestion. The most common symptoms include burning sensation and discomfort in the mouth and throat, difficulty swallowing, digestive disorders such as diffuse abdominal pain, nausea, vomiting, tenesmus, severe diarrhoea (in some cases bloody), resulting in dehydration (metabolic acidosis) and circulatory disorders (hypotension), which together can lead to hypovolaemic shock. Peripheral leukocytosis has occasionally been observed.
After the first 24 hours and for up to 7 days, the signs of toxicity include confusion, alopecia, cardiac disorders (including arrhythmias and decreased cardiac output), renal and hepatic impairment, respiratory distress, hyperpyrexia and bone marrow suppression. These signs may progress to multi-organ failure accompanied by bone marrow aplasia, CNS toxicity, seizures,
coma, hepatocellular damage, rhabdomyolysis, respiratory distress, renal and cardiac damage and disseminated intravascular dissemination. Death is generally due to cardiorespiratory depression.
Patients who survive beyond 7 days after an overdose may experience alopecia, rebound
leukocytosis and stomatitis (about 10 days after the overdose).
TREATMENT:
Treatment of colchicine overdose should include the use of oral activated charcoal in adults who have ingested more than 0.1 mg/kg of body weight of colchicine during the one-hour period following its ingestion and also in children who have ingested any amount during a one-hour period.
Higher doses of activated charcoal may increase systemic elimination and may be considered in patients who have ingested more than 0.3 mg/kg of body weight.
There is no specific antidote for colchicine. Gastric lavage may be performed. Haemodialysis and haemoperfusion do not increase the elimination of colchicine. Treatment of overdose should include general supportive and symptomatic measures depending on the patient’s clinical condition, including monitoring of vital signs, ECG, haematological and biochemical values. Breathing assistance may be required. Circulation should be maintained and the water-electrolyte balance should be corrected.
In case of severe abdominal pain, 10 mg of morphine sulphate may be administered intramuscularly.
To aid with the management of delayed onset of symptoms, patients should be monitored carefully for at least 6 hours after overdose, or at least 12 hours if they have taken more than 0.3 mg/kg of body weight. After this time, asymptomatic patients can be discharged with the warning that if they notice gastrointestinal symptoms, they should return to the unit where they were treated.
5 - PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: M04AX. Other antigout preparations.
Colchicine is used for the relief of acute gout attacks and prophylaxis of acute flares. Colchicine is also indicated for the treatment of chronic gout and familial Mediterranean fever.
The mechanism of action of colchicine is not fully understood. Colchicine produces an immediate response in gout attacks, probably by reducing the inflammatory reaction caused by urate crystals. This effect is due to several actions, including a reduction in leukocyte motility.
Colchicine inhibits phagocytosis of urate microcrystals, with a reduction in lactic acid production, which maintains a normal local pH. Acidity favours the precipitation of urate crystals, which is what causes gout attacks.
Colchicine has no analgesic activity and no effect on plasma concentrations or elimination of uric acid. It also has antimitotic activity (stops or inhibits cell division in the metaphase and anaphase).
Colchicine has other pharmacological actions in animals: it alters neuromuscular function, increases gastrointestinal activity by neurogenic stimulation, increases sensitivity to CNS depressants, increases response to sympathomimetics, depresses the central respiratory centre,
produces vasoconstriction, causes hypertension by central vasomotor stimulation and decreases body temperature.
The AGREE (Acute Gout Flare Receiving Colchicine Evaluation) study, a multi-centre, double-blind, placebo-controlled trial, evaluated the proportion of patients who responded to the following colchicine treatment regimens:
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- Group 1: High-dose colchicine (1.2 mg followed by 0.6 mg/hour for 6 hours [total dose: 4.8 mg])
- Group 2: Low-dose colchicine (1.2 mg followed by 0.6 mg/hour for 1 hour [1.8 mg])
- Group 3: Placebo
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A total of 184 patients were included in the intention-to-treat analysis. The primary endpoint of the study was the proportion of patients who responded to treatment. A responder was defined as a patient with a ≥ 50 % reduction in pain perception within the 24 hours after the first dose of medication, without using rescue medication. In the low-dose group, 28 out of 74 people (37.8%) responded to treatment; in the high-dose group, 17 out of 52 patients (32.7%) responded to treatment; and in the placebo group, 9 out of 58 patients (15.5%) were responders (p=0.005 and p=0.034, respectively, vs placebo). During the first few hours of treatment, 23 patients (31.1%) took
rescue medication in the low-dose group (p=0.027 vs placebo), 18 patients (34.6%) in the high-dose group (p=0.103 vs placebo), and 29 patients (50%) in the placebo group. The low-dose group showed a similar adverse effect profile to the placebo group, with an Odds Ratio (OR) of 1.5 (95% confidence interval [95% CI]: 0.7-3.2). High-dose colchicine was significantly associated with diarrhoea, vomiting and other adverse effects compared to the use of low-dose colchicine or placebo.
In the high-dose group, 40 patients (76.9%) experienced diarrhoea (OR 21.3 [95% CI: 7.9-56.9]), 10 (19.2%) severe diarrhoea and 9 (17.3%) vomiting. In the low-dose colchicine group, 23.0% of the patients experienced diarrhoea (OR 1.9 [95% CI: 0.8-4.8]) and none had severe diarrhoea or vomiting.
Low-dose colchicine resulted in a maximum plasma concentration and efficacy comparable to high-dose colchicine for the treatment of acute gout attack, with a similar safety profile to placebo.
5.2 Pharmacokinetic properties
Colchicine is absorbed orally with an approximate bioavailability of 45%.
Approximately 39% binds to albumin and there is no direct relationship with concentration. It binds to all tissues, primarily the intestinal mucosa, liver, kidneys and spleen, with the exception of the myocardium, skeletal muscles and lungs.
It has been reported that colchicine crosses the placenta, and plasma levels in the foetus are approximately 15% of the maternal concentration. The concentration in breast milk is similar to the plasma concentration observed in the mother.
The mean volume of distribution can range from 2 to 8 l/kg. Colchicine is partially metabolised in the liver by demethylation to two major metabolites, 2-O-desmethylcolchicine and 3-O-desmethylcolchicine, and one minor metabolite, 10-O-desmethylcolchicine.
CYP3A4 is involved in the metabolism of colchicine. Plasma levels of the two major metabolites are less than 5% of those of colchicine. The pharmacological activity of these metabolites is unknown.
Colchicine and its metabolites undergo enterohepatic circulation.
In patients with severe hepatic impairment, its clearance is significantly decreased and its half-life is prolonged. In patients with mild to moderate hepatic impairment, the data show a high degree of inter-patient variability.
Renal clearance of colchicine has been estimated to be 0.727 l/h/kg in patients with good renal function. In patients with severe renal impairment, renal clearance was reduced by 75%. There are no data in patients with mild to moderate renal impairment.
Colchicine is not eliminated by haemodialysis.
The elimination half-life in healthy volunteers described in the literature (aged between 25 and 28 years) ranges from 26.6 to 31.2 hours.
Colchicine is a P-glycoprotein substrate.
No differences in pharmacokinetics have been described according to sex.
The pharmacokinetics in paediatric patients have not been described.
According to a published study in elderly patients, the mean plasma peak and AUC were twice as high as in young subjects. The explanation for this difference may be lower renal function.
5.3 Preclinical safety data
Available non-clinical data did not show any risks in humans other than those expected based on the established conditions of administration. However, colchicine was found to be teratogenic in animals.
6 - PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Lactose, microcrystalline cellulose, povidone, methylene casein, magnesium stearate and erythrosine lake.
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
5 years.
6.4 Special precautions for storage
This medicine does not require any special storage conditions.
6.5 Nature and contents of container
Carton containing 2 blisters with 20 tablets each.
6.6 Special precautions for disposal
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
7 - MARKETING AUTHORISATION HOLDER
SEID, S.A.
Carretera de Sabadell a Granollers, Km. 15 08185 Lliçà de Vall (Barcelona). Spain
8 - MARKETING AUTHORISATION NUMBER
33.720
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
12 May 1960
10. DATE OF REVISION OF THE TEXT
January 2011
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