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CrossRef citations to date Dihydrocodeine (DHC) is a semi-synthetic analogue of codeine, which was formed by In patients with postoperative pain after subcutaneous administration of 30 mg DHC analgesia was similar. Order. Home / Dihydrocodeine 30mg tablets | tablet | Newsletter sign up. Email address: Date of birth: Gender: Location: Leave this field empty if you're. Taken orally, this has about the same effect as taking 20 to 30mg of But I could buy as much codeine or dihydrocodeine as I liked from.
Do not use this medicine to treat any other complaint unless your doctor says it is safe. Comfarol Forte is not recommended for children under 7 years. Before you start to take it Tell your doctor or pharmacist if you have allergies to: Tell your doctor or pharmacist if you have or have had any medical conditions, especially the following: Tell your doctor if you are pregnant or are planning to become pregnant.
Comfarol Forte may be used during pregnancy. However, it is recommended that non-drug therapies such as rest and massage be tried first. If you have not told your doctor about any of these things, tell them before you take any Comfarol Forte. Taking other medicines You should also tell your doctor about any other medicines that you have bought without a prescription from either your pharmacy, supermarket or health food shop. Tell your doctor if you are using any other medicines, including any of the following medicines: These medicines may be affected by Comfarol Forte or may affect how well Comfarol Forte works.
Your doctor or pharmacist can tell you what to do if you are taking any of these medicines. How to take Comfarol Forte The label on your pack of Comfarol Forte will tell you how to take your medicine and how often.
If you are unsure about the directions ask your doctor or pharmacist.
Do not take more than the dose your doctor or pharmacist has directed. The dosage recommended by the doctor may be different to the recommended dosage.
The recommended dose of Comfarol Forte is: This dosage may be repeated in hours if necessary. Do not take more than 8 tablets in 24 hours. Do not take more than the recommended dose.
Taking more than the recommended dose may cause liver damage. Talk to your doctor about pain control if the medicine is not helping. If your body cannot metabolise codeine properly, you may be getting reduced benefit from the medicine. Children should not take more than 3 tablets in 24 hours. How to take it Swallow the tablets with water. The directions given to you by your doctor or pharmacist may be different from the information in this leaflet.
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If you are unsure what dose to take ask your pharmacist or doctor. If you forget to take it If it is almost time for your next dose, skip the dose you missed and take your next dose when you are meant to. Otherwise, take it as soon as you remember, and then go back to taking your medicine as you would normally. Do not take a double dose to make up for the dose that you missed.
This may increase the chance of you getting an unwanted side effect. If you are not sure what to do, ask your pharmacist or doctor.
If you take too much Overdose Immediately telephone your doctor or Poisons Information Centre telephone 13 11 26 for advice, or go to Accident and Emergency at your nearest hospital, if you think that you or anyone else has taken too much Comfarol Forte. Do this even if there are no signs of discomfort or poisoning. You may need urgent medical attention. Keep telephone numbers of these places handy. If you take too many tablets you may feel nauseous, light headed, dizzy or drowsy. Tell all your doctors, dentists and pharmacists that you are taking Comfarol Forte.
Dihydrocodeine Tablets BP 30mg - Patient Information Leaflet (PIL) - (eMC)
Tell your doctor if you become pregnant while taking Comfarol Forte. Things you must not do Do not take more than the recommended dose unless your doctor tells you to.
Dihydrocodeine may delay absorption of mexiletine. The analgesic activity of dihydrocodeine may be significantly impaired by quinidine which impairs codeine metabolism. Antidepressants, anxiolytics, hypnotics and antipsychotics: Opiates potentiate the effects of CNS depressants, including anxiolytics e.
MAOIs taken with pethidine have been associated with severe CNS excitation or depression including hypertension or hypotension. Although this has not been documented with dihydrocodeine, it is possible that a similar interaction may occur and therefore the use of dihydrocodeine should be avoided while the patient is taking MAOIs and for 2 weeks after MAOI discontinuation.
Antidiarrhoeal and antiperistaltic agents e. Dihydrocodeine has an antagonistic effect on cisapride, metoclopramide and domperidone.
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Cimetidine may inhibit the metabolism of dihydrocodeine resulting in increased plasma concentrations. Interference with laboratory tests: Opioids may interfere with gastric emptying studies as they delay gastric emptying and with hepatobiliary imaging using technetium Tc 99m disofenin as opioid treatment may cause constriction of the sphincter of Oddi and increase biliary tract pressure.
Dihydrocodeine may cause respiratory depression in the neonate. Opioid analgesics may cause withdrawal effects in neonates of dependant mothers and gastric stasis during labour, increasing the risk of inhalation pneumonia. It is not known if dihydrocodeine is excreted into breast milk and use should be avoided during breast-feeding unless the potential benefit outweighs the risk. If affected, patients should not drive or operate machinery.
The effects of alcohol are enhanced by opioid analgesics. 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 of Traffic Act When prescribing this medicine, patients should be told: Symptoms of restlessness and irritability may result when treatment is then stopped.
Prolonged use of a painkiller for headaches can make them worse. Raised intracranial pressure may occur in some patients.
Ear and labyrinth disorders: Large doses produce hypotension. Respiratory, thoracic and mediastinal disorders: Larger doses produce respiratory depression. Biliary spasm may be associated with altered liver enzyme values. Skin and subcutaneous tissue disorders: Musculoskeletal and connective tissue disorders: Muscle rigidity may occur after high doses.
Renal and urinary disorders: