Codeine linctus bp health
Keep out of the sight and reach of children. This product contains 4g of sucrose per dose. To be taken into account in people with diabetes. It also contains invert syrup. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine. It contains a small amount of ethanol alcohol , less than mg per 5ml. Metabolism of codeine is accelerated by rifampicin leading to reduced effect.
As an opioid analgesic, codeine phosphate may potentiate the effects of tranquillisers such as barbiturates, general anaesthetics, anxiolytics and hypnotics, sedatives and alcohol. Possible CNS excitation or depression hypertension or hypotension can occur when opioid analgesics are given with antidepressants such as moclobemide a reversible MAO-A inhibitor. The sedative effects of codeine can possibly be increased when given with tricyclic antidepressants, with anxiolytics or hypnotics, or with sedating antihistamines.
Antipsychotic medicines can enhance hypotensive and sedative effects when opioid analgesics are given with antipsychotics. MAOIs taken with pethidine have been associated with severe CNS excitation or depression including hypertension or hypotension. Although this has not been documented with codeine, it is possible that a similar interaction may occur and therefore the use of codeine should be avoided while the patient is taking MAOIs and for 2 weeks after MAOI discontinuation, including MAO-B inhibitor selegiline.
This may also apply to the antibacterial linezolid, which is a reversible, non-selective MOA inhibitor. The reduction in intestinal motility caused by codeine may delay the absorption or antagonise the gastrointestinal effects of other drugs e.
Metabolism of opioid analgesics is inhibited by cimetidine leading to increased plasma concentration. May delay the gastro-intestinal absorption of mexiletine or quinidine which may also reduce the efficacy of codeine.
Opioid analgesics enhance the effects of sodium oxybate, used to treat symptoms of narcolepsy, and concomitant use should be avoided. Opioid administration in the third trimester may cause respiratory depression in the newborn, withdrawal effects in neonates of dependent mothers, gastric stasis and risk of inhalation pneumonia in the mother during labour.
Codeine should not be used during breastfeeding see section 4. At normal therapeutic doses codeine and its active metabolite may be present in breast milk at very low doses and is unlikely to adversely affect the breast fed infant.
However, if the patient is an ultrarapid metaboliser of codeine higher levels of the active metabolite, morphine, may be present in breast milk and on very rare occasions may result in symptoms of opioid toxicity in the infant, which may be fatal. The infant itself may be a CYP2D6 ultra-rapid metaboliser. In either case on very rare occasions this may result in symptoms of opioid toxicity in the infant.
See also section 4. If symptoms of opioid toxicity develop in either the mother or the infant, then all codeine containing medicines should be stopped and alternative non-opioid analgesics prescribed. In severe cases consideration should be given to prescribing naloxone to reverse these effects.
This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act When prescribing this medicine, patients should be told: Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.
Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at www. Gastric lavage should be carried out and a saline purgative may then be given to reduce absorption from gastro — intestinal tract.
Symptomatic treatment of respiratory embarrassment should be given. If respiration is seriously depressed intravenous naloxone HCl may be required. Antitussive — suppresses the cough reflex by a direct central action, probably in the medulla or pons. Codeine is a centrally acting weak analgesic.
Codeine, particularly in combination with other analgesics such as paracetamol, has been shown to be effective in acute nociceptive pain. Half life from 2. Duration of action approximately 4 hours. Onset of action after oral administration is 30 to 45 minutes.
Promethazine
Information for consumers 23 May On 8 Februarycodeine linctus bp health, the TGA published safety information for consumers regarding Pradaxa active ingredient dabigatran. Sunset Yellow may cause allergic reactions. The infant itself may be a CYP2D6 ultra-rapid metaboliser, codeine linctus bp health. The sedative effects of codeine can possibly be increased when given with tricyclic antidepressants, with anxiolytics or hypnotics, or with sedating antihistamines. However, a number of people in Australia have linctus the product … Beast Amphetalean powder 13 May Beast Amphetalean powder poses a serious risk to your health and should not be taken. It contains a small health of ethanol alcoholless than mg per 5ml. Antipsychotic codeines can enhance hypotensive and sedative effects when codeine analgesics are given with antipsychotics. To be taken into account in people with diabetes. Codeine should not be used during breastfeeding see section 4. Codeine is a centrally acting weak analgesic. The packaging states the goods are capsules, however … Extra Power powder sachets 29 August Extra Power health sachets vicodin potassium levels a serious risk to your health, and should not be taken.
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