Co-Dydramol Tablets Bp
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Co-dydramol Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains Dihydrocodeine TartratelO mg & Paracetamol 500 mg. For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
White, flat bevel edged tablet engraved with company logo on one face and A476 and a bar on the other face.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Analgesic for the relief of mild to moderate pain.
4.2 Posology and method of administration Posology:
Adults and Children over 16 years
Initially one or, if necessary, two tablets every 4 hours to a maximum of 8 tablets daily.
Children between 12 and 15 years old
1 tablet every 4-6 hours when necessary to a maximum of 4 doses in 24 hours.
Children under 12 years old
Not recommended for children under 12 years.
Elderly
Dosage should be reduced in the elderly.
Method of Administration
For oral administration.
It is recommended that this product should be taken during or after meals.
4.3 Contraindications
• Hypersensitivity to dihydrocodeine tartrate, other opioids or paracetamol or to any of the excipients listed in section 6.1;
• Respiratory depression;
• Obstructive airways disease;
• Diarrhoea caused by poisoning until the toxic material has been eliminated, or diarrhoea associated with pseudomembraneous colitis.
4.4 Special warnings and precautions for use
Co-dydramol should be used with caution in patients with:
• Hepatic function impairment (avoid if severe) and those with non-cirrhotic alcoholic liver disease. The hazards of overdose are greater in those with alcoholic liver disease;
• Prolonged use of co-dydramol may cause hepatic necrosis;
• Renal function impairment;
• Hypothyroidism (risk of depression and prolonged CNS depression is increased);
• Inflammatory bowel disease - risk of toxic megacolon;
• Opioids should not be administered during an asthma attack;
• Convulsions - may be induced or exacerbated;
• Drug abuse, dependence (including alcoholism), enhanced instability, suicidal ideation or attempts - predisposed to drug abuse;
• Head injuries or conditions where intracranial pressure is raised;
• Gall bladder disease or gall stones - opioids may cause biliary contraction
• Gastro-intestinal surgery - use with caution after recent GI surgery as opioids may alter GI motility;
• Prostatic hypertrophy or recent urinary tract surgery;
• Adrenocortical insufficiency, eg Addison's Disease;
• Hypotension and shock;
• Myasthenia gravis;
• Phaeochromocytoma - opioids may stimulate catecholamine release by
inducing the release of endogenous histamine.
Where analgesics are used long-term (>3 months) with administration every two days or more frequently, headache may develop or worsen. Headache induced by overuse of analgesics (MOH medication-overuse headache) should not be treated by dose increase. In such cases, the use of analgesics should be discontinued in consultation with the doctor.
The label will have the following warnings:
• Do not take with anything else containing paracetamol while taking this medicine.
• Contains paracetamol.
• Talk to your doctor at once if you take too much of this medicine, even if you feel well.
• Do not take more medicine than the label tells you to. If you do not get better, talk to you doctor.
The label will also state (to be displayed prominently on outer pack - not boxed):
• Do not take for longer than directed by your prescriber as taking dihydrocodeine regularly for a long time can lead to addiction.
The leaflet will state in a prominent position in the “before taking” section:
• Do not take for longer than directed by your prescriber.
• Taking dihydrocodeine regularly for a long time can lead to addiction, which might cause you to feel restless and irritable when you stop the tablets.
• Taking a painkiller for headaches too often or for too long can make them worse.
• Talk to your doctor at once if you take too much of this medicine, even if you feel well. This is because too much paracetamol can cause delayed, serious liver damage.
4.5 Interaction with other medicinal products and other forms of interaction Paracetamol can interact with the following:
• Drugs which alter gastric emptying time (e.g. cimetidine, ethyl alcohol, oral steroid contraceptives). These drugs reduce or delay peak paracetamol blood levels;
• Metoclopramide or domperidone increases the speed of absorption of paracetamol;
• Colestyramine reduces paracetamol absorption;
• Drugs which interfere with the metabolism of paracetamol by competition with metabolic pathways or substrates e.g. anticonvulsants (phenytoin), hepatic enzyme inducers, alcohol, barbiturates, tricyclic antidepressants. A poor diet (low protein) may also have a similar effect on the risk of serious paracetamol toxicity to hepatic enzyme inducers. Patients who have taken barbiturates, tricyclic antidepressants and alcohol may show diminished ability to metabolise large doses of paracetamol, the plasma half-life of which may be prolonged;
• The anticoagulant effect of warfarin and other coumarins may be enhanced by prolonged regular use of paracetamol with increased risk of bleeding;
• Alcohol can increase the hepatotoxicity of paracetamol overdosage and may have contributed to the acute pancreatitis reported in one patient who had taken an overdosage of paracetamol.
Dihydrocodeine can interact with the following:
• CNS depressants - enhanced sedative and/or hypotensive effect with alcohol, anaesthetics, hypnotics, anxiolytics, antipsychotics, hydroxyzine, tricyclic antidepressants;
• Antibacterials, e.g. ciprofloxacin, - avoid premedication with opioids as reduced plasma ciprofloxacin concentration;
• MAOIs - use only with extreme caution;
• Cyclizine;
• Mexiletine - delayed absorption;
• Metoclopramide and domperidone - antagonise GI effects;
• Cisapride - possible antagonism of GI effects;
• Dopaminergics (e.g. selegiline) - possible risk of hyperpyrexia and CNS toxicity. This risk is greater with pethidine but with other opioids the risk is uncertain;
• Ulcer healing drugs - cimetidine inhibits the metabolism of opioid analgesics;
• Anticholinergics (e.g. atropine) - risk of severe constipation which may lead to paralytic illness, and/or urinary retention;
• Antidiarrhoeal drugs (e.g. loperamide, kaolin) - increased risk of severe constipation;
• Antihypertensive drugs (e.g. guanethidine, diuretics) - enhanced hypotensive effect;
• Opioid antagonists (e.g. buprenorphine, naltrexone, naloxone);
Neuromuscular blocking agents - additive respiratory depressant effects.
4.6 Fertility, pregnancy and lactation
Pregnancy
Epidemiological studies in human pregnancy have shown no ill effects due to paracetamol used in the recommended therapeutic dosage. However, paracetamol should be avoided in pregnancy unless considered essential by the physician.
Risk benefit must be considered because opioid analgesics cross the placenta. Studies in animals have shown opioids to cause delayed ossification in mice and increased resorption in rats.
Regular use during pregnancy may cause physical dependence in the fetus, leading to withdrawal symptoms in the neonate.
During labour opioids enter the fetal circulation and may cause respiratory depression in the neonate. Administration should be avoided during the late stages of labour and during the delivery of a premature infant.
Breast-feeding
Paracetamol is excreted in breast milk but not in a clinically significant amount. Available published data do not contraindicate breast-feeding, however some opioids are distributed in breast milk in small amounts and it is advisable to avoid administration opioids in a breastfeeding woman.
4.7 Effects on ability to drive and use machines
Opioid analgesics can impair mental function and can cause blurred vision and dizziness. Patients should make sure they are not affected before driving or operating machinery.
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:
- The medicine has been prescribed to treat a medical or dental problem and
- You have taken it according to the instructions given by the prescriber and in the information provided with the medicine and
- It was not affecting your ability to drive safely
4.8 Undesirable effects
At the recommended dosage, paracetamol may cause the following side
effects:
• Allergic reactions - rare but may include skin rash, drug fever, mucosal lesions;
• Effects on the skin - Very rare cases of serious skin reactions have been reported;
• Effects on CNS - drowsiness, impaired mental functions;
• Effects on GI system - Chronic hepatic necrosis has been reported in a patient who took daily therapeutic doses of paracetamol for about a year, and liver damage has been reported after daily ingestion of excessive amounts for shorter periods. Acute pancreatitis has been reported. A review of a group of patients with chronic active hepatitis failed to reveal differences in the abnormalities of liver function in those who were longterm users of paracetamol, nor was the control of their disease improved after paracetamol withdrawal;
• Effects on CVS - toxic myocarditis;
• Effects on blood - methaemoglobinaemia, neutropenia, pancytopenia, leukopenia, thrombocytopenic purpura, haemolytic anaemia and agranulocytosis;
• Effects on GU system - Nephrotoxicity following therapeutic doses of paracetamol is uncommon, but papillary necrosis has been reported after prolonged administration;
• Other effects - Most reports of adverse reactions to paracetamol relate to overdosage with the drug.
Adverse effects of opioid treatment which have been reported include:
• Allergic reactions (may be caused by histamine release) - including rash, urticaria, difficulty breathing, increased sweating, redness or flushed face;
• Effects on CNS - confusion, drowsiness, vertigo, dizziness, changes in mood, hallucinations, CNS excitation (restlessness/excitement), convulsions, mental depression, headache, trouble sleeping, or nightmares, raised intracranial pressure, tolerance or dependence;
• Effects on GI system - constipation, GI irritation, biliary spasm, nausea, vomiting, loss of appetite, dry mouth, paralytic ileus or toxic megacolon;
• Effects on CVS - bradycardia, palpitations, hypotension;
• Effects on sensory system - blurred or double vision;
• Effects on GU system - ureteral spasm, antidiuretic effect;
• Other effects - trembling, unusual tiredness or weakness, malaise, miosis, hypothermia;
• Effects of withdrawal - abrupt withdrawal precipitates a withdrawal syndrome. Symptoms may include tremor, insomnia, nausea, vomiting, sweating and increase in heart rate, respiratory rate and blood pressure. NOTE - tolerance diminishes rapidly after withdrawal so a previously tolerated dose may prove fatal;
• Regularly prolonged use of dihydrocodeine is known to lead to addiction and tolerance. Symptoms of restlessness and irritability may result when treatment is then stopped.
• Prolonged use of a painkiller for headaches can make them worse. Reporting of side effects
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. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard.
4.9 Overdose
Paracetamol:
Liver damage is possible in adults who have taken 10g or more of paracetamol. Ingestion of 5g or more of paracetamol may lead to liver damage if the patient has risk factors (see below).
Risk factors:-If the patient
• Is on long term treatment with carbamazepine, phenobarbital, phenytoin, primidone, rifampicin, St John’s Wort or other drugs that induce liver enzymes.
• Regularly consumes ethanol in excess of recommended amounts.
• Is likely to be glutathione deplete e.g. eating disorders, cystic fibrosis, HIV infection, starvation, cachexia.
Symptoms:-
Symptoms of paracetamol overdosage in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain. Liver damage may become apparent 12 to 48 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur. In severe poisoning, hepatic failure may progress to encephalopathy, haemorrhage, hypoglycaemia, cerebral oedema, coma and death. Acute renal failure with tubular necrosis, strongly suggested by loin pain, haematuria and proteinuria, may develop even in the absence of severe liver damage. Cardiac arrhythmias and pancreatitis have been reported.
Managament
Immediate treatment is essential in the management of paracetamol overdose. Despite a lack of significant early symptoms, patients should be referred to hospital urgently for immediate medical attention. Symptoms may be limited to nausea or vomiting and may not reflect the severity of overdose or the risk of organ damage. Management should be in accordance with established treatment guidelines, see BNF overdose section.
Treatment with activated charcoal should be considered if the overdose has been taken within 1 hour. Plasma paracetamol concentration should be measured at 4 hours or later after ingestion (earlier concentrations are unreliable). Treatment with N-acetylcysteine may be used up to 24 hours after ingestion of paracetamol, however, the maximum protective effect is obtained up to 8 hours post-ingestion. The effectiveness of the antidote declines sharply after this time. If required the patient should be given intravenous N-acetylcysteine, in line with the established dosage schedule. If vomiting is not a problem, oral methionine may be a suitable alternative for remote areas, outside hospital. Management of patients who present with serious hepatic dysfunction beyond 24 hours from ingestion should be discussed with the NPIS or a liver unit.
Dihydrocodeine
Symptoms
Acute overdosage with dihydrocodeine can be manifested by somnolence progressing to stupor or coma, miotic pupils, rhabdomyolysis, non-cardiac pulmonary oedema, bradycardia, hypotension and respiratory depression or apnoea.
Management
Primary attention should be given to the establishment of a patent airway and institution of assisted or controlled ventilation.
In the case of massive overdosage, administer naloxone intravenously (0.4 to 2 mg for an adult and 0.01 mg/kg body weight for children) if the patient is in a coma or respiratory depression is present. Repeat the dose at 2 minute intervals if there is no response, or by an infusion. An infusion of 60% of the initial dose per hour is a useful starting point. A solution of 10 mg made up in 50 ml dextrose will produce 200 micrograms/ml for infusion using an IV pump (dose adjusted to the clinical response). Infusions are not a substitute for frequent review of the patient's clinical state. Intramuscular naloxone is an alternative in the event that IV access is not possible.
As the duration of action of naloxone is relatively short, the patient must be carefully monitored until spontaneous respiration is reliably re-established. Naloxone is a competitive antagonist and large doses (4 mg) may be required in seriously poisoned patients. For less severe overdosage, administer naloxone 0.2 mg intravenously followed by increments of 0.1 mg every 2 minutes if required.
Naloxone should not be administered in the absence of clinically significant respiratory or circulatory depression secondary to dihydrocodeine overdosage. Naloxone should be administered cautiously to persons who are known, or suspected, to be physically dependent on dihydrocodeine. In such cases, an abrupt or complete reversal of opioid effects may precipitate pain and an acute withdrawal syndrome.
Consider activated charcoal (50 g for adults, 10-15 g for children), if an adult presents within 1 hour of ingestion of more than 420mg or a child more than 3mg/kg.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Dihydrocodeine tartrate is an opioid analgesic.
Paracetamol has analgesic and antipyretic properties.
5.2 Pharmacokinetic properties
Dihydrocodeine is absorbed from the gastrointestinal tract. Dihydrocodeine is metabolised by O- and N-demethylation in the liver to morphine, norcodeine and other metabolites. It is excreted almost entirely by the kidney, mainly as conjugates with glucoric acid. Paracetamol is readily absorbed from the gastrointestinal tract with peak plasma concentrations occurring about 10-60 minutes after ingestion. Paracetamol is distributed into most body tissues. It crosses the placenta and is present in breast milk. Plasma-protein binding is negligible at usual therapeutic concentrations but increases with increasing concentrations.
Paracetamol is metabolised predominantly in the liver and excreted in the urine mainly as the glucoronide and sulphate conjugates. Less than 5% is excreted as unchanged paracetamol. A minor hydroxylated metabolite which is usually produced in very small amounts by mixed-function oxidases in the liver and which is usually detoxified by conjugation with liver glutathione may accumulate following paracetamol overdosage and cause tissue damage. The elimination half-life varies from about 1-3 hours.
5.3 Preclinical safety data
There are no pre-clinical data of relevance to the prescriber which are additional to that covered in other sections of the SPC.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
• Starch;
• Polyvinylpyrrolidone;
• Sodium Starch Glycollate;
• Stearic Acid;
• Colloidal Silicon Dioxide;
• Talc;
• Potable Water.
6.2 Incompatibilities
None.
6.3 Shelf life
36 months for opaque plastic containers.
24 months for blisters.
6.4 Special precautions for storage
Store below 25°C. Protect from light and moisture. Keep out of the sight and reach of children.
6.5 Nature and contents of container
Co-Dydramol tablets are packed in the following containers and closures and pack sizes.
Opaque plastic containers composed of polypropylene tubes fitted with polyethylene made tamper-evident closures in pack sizes of 10, 12, 20, 24, 25, 30, 50, 100, 250, 500 and 1,000 tablets.
Opaque plastic containers composed of either, high density polypropylene or high density polyethylene with a tamper evident or child resistant tamper evident closure composed of high density polyethylene in pack sizes of 10, 12, 20, 24, 25, 30, 50, 100, 250, 500 and 1,000 tablets.
Blister packs of 20pm hard aluminium foil laminated to 15 pm rigid PVC film, and 250pm white opaque PVC film, containing 30 and 100 tablets.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal and other handling
Not applicable.
7 MARKETING AUTHORISATION HOLDER
Bristol Laboratories Limited Unit 3, Canalside,
Northbridge road,
Berkhamsted HP4 1EG United Kingdom
8 MARKETING AUTHORISATION NUMBER(S)
PL 17507/0195
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
28 July 2004
10 DATE OF REVISION OF THE TEXT
26/09/2016