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Codeine Phosphate in Boots chemist - Bangkok Forum - TripAdvisor

Codeine in boots - Further information

It could be helpful to inform friends or relatives to be aware of the signs and symptoms stated above. Contact your doctor when experiencing such symptoms How to take this medicine Check the foil is not broken before use.

If it is, do not take that tablet. Dissolve the tablets in a glass of water and then drink the solution. Adults over 18 years — Two tablets to be dissolved in water — Take every 4 to 6 hours, if you need to up to 4 times in 24 hours.

DO NOT take more than 8 tablets in 24 hours. Children aged 16 to 18 years — One or two tablets to be dissolved in water — Take every 6 hours, if you need to up to 4 times in 24 hours. Children aged 12 years to 15 years — One tablet to be dissolved in water — Take every 6 hours, if you need to up to 4 times in 24 hours. DO NOT take more that 4 tablets in 24 hours. DO NOT take more often than every 4 hours. Do not take for more than 3 days.

If you need to use this medicine for more than 3 days you must speak to your doctor or pharmacist for advice. Do not give to children under 12 years, due to the risk of severe breathing problems. Do not take more than the amount recommended in the table. If you do not get better, talk to your doctor. If you take too many tablets: Talk to a 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. Go to your nearest hospital casualty department. Take your medicine and this leaflet with you. Possible withdrawal effects when stopping treatment This medicine contains codeine and can cause addiction if you take it continuously for more than 3 days.

When you stop taking it you may get withdrawal symptoms. You should talk to your doctor or pharmacist if you think you are suffering from withdrawal symptoms. Possible side effects Most people will not have problems, but some people may have side effects when taking this medicine. If you have any unwanted side effects you should seek advice from your doctor, pharmacist or other healthcare professional. If you get any of these serious side effects, stop taking the tablets. See a doctor at once: Difficulty in breathing, swelling of the face, neck, tongue or throat severe allergic reactions Very rare cases of serious skin reactions have been reported.

This may include peeling, blistering and lesions of the skin. Severe stomach pain, which may reach through to the back. This may be a sign of pancreatitis, which is very rare If you get any of the following side effects see your pharmacist or doctor: Constipation, feeling sick, being sick, stomach upset Drowsiness, dizziness, feeling light headed, headache - do not drive or use machines if you feel drowsy or dizzy Difficulty in passing urine Feeling shaky or shaking, fast heart rate Difficulty sleeping Other allergic reactions e.

This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: By reporting side effects you can help provide more information on the safety of this medicine.

How do I know if I am addicted? If you take the medicine according to the instructions on the pack it is unlikely that you will become addicted to the medicine. However, if the following apply to you it is important that you talk to your doctor: Store in the original package to help protect from moisture.

Keep this medicine in a safe place out of the sight and reach of children, preferably in a locked cupboard. Use by the date on the end flap of the carton. What is in this medicine Each effervescent tablet contains Caffeine 30 mg, Codeine Phosphate 8 mg, Paracetamol mg which are the active ingredients. As well as the active ingredients, the tablets also contains sorbitol E , saccharin sodium, sodium bicarbonate, povidone, sodium laurilsulfate, citric acid anhydrous, sodium carbonate, dimeticone.

This pack contains 32 flat white tablets with bevelled edges, plain on one side, scored on the other side. In animals, administration of a prostaglandin synthesis inhibitor has been shown to result in increased pre- and post-implantation loss and embryo-foetal lethality.

In addition, increased incidences of various malformations, including cardiovascular, have been reported in animals given a prostaglandin synthesis inhibitor during the organogenetic period. During the first and second trimester of pregnancy, acetylsalicylic acid should not be given unless clearly necessary. If acetylsalicylic acid is used by a woman attempting to conceive, or during the first and second trimester of pregnancy, the dose should be kept as low and duration of treatment as short as possible.

During the third trimester of pregnancy, all prostaglandin synthesis inhibitors may expose the foetus to: As aspirin is secreted into breast milk in low concentrations, use of aspirin and codeine tablets should be avoided during lactation because of the risk of Reye's syndrome and the fact that high doses of aspirin could potentially impair platelet function.

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 ultra-rapid metaboliser of CYP2D6, 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.

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: Less commonly irritation of the gastrointestinal mucosa may lead to erosion, ulceration, gastrointestinal bleeding. Hepatotoxicity which occurs rarely. Aspirin may precipitate bronchospasm and induce asthma attacks or other hypersensitivity reactions including urticaria, rhinitis and angioneurotic oedema in susceptible individuals.

Aspirin may also cause salt and water retention as well as deterioration in renal function see also section 4. Regular prolonged use of codeine is known to lead to addiction and 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 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: Common features of salicylate poisoning include vomiting, dehydration, tinnitus, vertigo, deafness, sweating, warm extremities with bounding pulses, increased respiratory rate and hyperventilation. Some degree of acid-base disturbance is present in most cases.

A mixed respiratory alkalosis and metabolic acidosis with normal or high arterial pH normal or reduced hydrogen ion concentration is usual in adults and children over the age of 4 years. In children aged 4 years or less, a dominant metabolic acidosis with low arterial pH raised hydrogen ion concentration is common. Acidosis may increase salicylate transfer across the blood brain barrier. Central nervous system features including confusion, disorientation, coma and convulsions are less common in adults than in children.

The plasma salicylate concentration should be measured, although the severity of poisoning cannot be determined from this alone and the clinical and biochemical features must be taken into account. Elimination is increased by urinary alkalinisation, which is achieved by the administration of 1. The urine pH should be monitored. Correct metabolic acidosis with intravenous 8. Forced diuresis should not be used since it does not enhance salicylate excretion and may cause pulmonary oedema.

Patients under 10 years or over 70 have increased risk of salicylate toxicity and may require dialysis at an earlier stage. The effects of codeine in overdosage will be potentiated by simultaneous ingestion of alcohol and psychotropic drugs.

Boots Paracetamol and Codeine Extra

In animals, administration of a prostaglandin synthesis inhibitor has been shown to result in increased pre- and post-implantation loss and embryo-foetal lethality. Aspirin may precipitate bronchospasm and induce asthma attacks or other hypersensitivity reactions including urticaria, rhinitis and angioneurotic oedema in susceptible individuals. Keep this medicine in a safe place out of the sight and reach of children, codeine in boots, preferably in a locked codeine. You can also report side effects directly via the Yellow Card Scheme at: The toxicity of methotrexate may be enhanced by concomitant use of aspirin. Codeine should not be used during breastfeeding see section 4. Codeine may delay the absorption of mexiletine and thus reduce the antiarrhythmic effect of the latter. Benzodiazepines — used for codeine anxiety or sleep disorders Domperidone or metoclopramide for boot sick or boot sick may increase the pain relief effect of paracetamol Colestyramine for reducing blood fat levels may reduce the pain relief effect of paracetamol Warfarin or other blood thinners - if you take warfarin you can take occasional amounts of this medicine, but talk to your doctor first before you take it on a regular basis If you are unsure about interactions with any other medicines, codeine in boots, talk to your pharmacist. However, if the following apply to you it is important that you talk to your doctor: If acetylsalicylic acid is used by a woman attempting to conceive, or during the first and second trimester of pregnancy, the dose should be kept as low and duration of treatment as short as possible, codeine in boots. In children aged 4 years or less, a dominant metabolic acidosis with low arterial pH raised boot ion concentration is common. As aspirin is secreted into breast milk in low concentrations, use of aspirin and codeine boots should be avoided during codeine because of the risk of Reye's syndrome and the fact that high doses of aspirin could potentially impair platelet function, codeine in boots. Some aspirin is hydrolysed to salicylate in the gut wall. Children with compromised respiratory function Codeine is not recommended for use in codeines in whom respiratory function might be compromised including neuromuscular disorders, severe cardiac or respiratory conditions, upper respiratory or lung infections, multiple trauma or extensive surgical procedures. Aspirin diminishes the uricosuric action of probenecid and sulphinpyrazone.


Boots Paracetamol and Codeine

codeine in bootsPossible side effects Most people will not have problems, but some people may have side effects when taking this medicine, codeine in boots. Codeine belongs to a boot of medicines called opioid analgesics which oxycodone apap 5mg-325mg information to relieve pain. As a result of zero order kinetics, plasma steady state salicylate concentrations increase disproportionately with dose. If acetylsalicylic acid is used by a woman attempting to conceive, codeine in boots, or during the first and second trimester of pregnancy, the dose should be kept as low and boot of treatment as short as possible. This class of medicine is in the list of drugs included in regulations under 5a of the Road Traffic Act Hepatotoxicity which occurs rarely. Constipation, codeine sick, being sick, stomach upset Drowsiness, dizziness, feeling light headed, headache - do not drive or use machines if you feel drowsy or dizzy Difficulty in passing urine Feeling shaky or shaking, codeine heart rate Difficulty sleeping Other allergic reactions e, codeine in boots. Elimination is increased by urinary alkalinisation, which is achieved by the administration of 1. Codeine phosphate is absorbed from the gastrointestinal tract and peak boot concentrations occur after about one hour. This may include peeling, blistering and lesions of the skin. If you take other medicines This medicine contains paracetamol. As well as the active ingredients, the tablets also contains sorbitol Ecodeine sodium, sodium codeine, povidone, sodium laurilsulfate, citric boot anhydrous, sodium carbonate, dimeticone.


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