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  2. Hydrocodone/paracetamol - Wikipedia

    en.wikipedia.org/wiki/Hydrocodone/paracetamol

    The panel also cited concerns of liver damage from their paracetamol component, which is also the main ingredient in commonly used nonprescription drugs such as Tylenol. [21] Each year, paracetamol overdose is linked to about 400 deaths and 42,000 hospitalizations. [22]

  3. Pethidine - Wikipedia

    en.wikipedia.org/wiki/Pethidine

    Pethidine is the preferred painkiller for diverticulitis, because it decreases intestinal intraluminal pressure. [19] Pethidine is the preferred drug for the management of shivering during therapeutic hypothermia , as it provides the greatest reduction in the shivering threshold.

  4. Naloxegol - Wikipedia

    en.wikipedia.org/wiki/Naloxegol

    Naloxegol (INN; PEGylated naloxol; [4] trade names Movantik and Moventig) is a peripherally acting μ-opioid receptor antagonist developed by AstraZeneca, licensed from Nektar Therapeutics, for the treatment of opioid-induced constipation. [5] It was approved in 2014 in adult patients with chronic, non-cancer pain. [6]

  5. Nimesulide - Wikipedia

    en.wikipedia.org/wiki/Nimesulide

    Nimesulide is a nonsteroidal anti-inflammatory drug (NSAID) with pain medication and fever reducing properties. Its approved indications are the treatment of acute pain, the symptomatic treatment of osteoarthritis, and primary dysmenorrhoea in adolescents and adults above 12 years old.

  6. Ibuprofen - Wikipedia

    en.wikipedia.org/wiki/Ibuprofen

    Example of some 200 mg ibuprofen tablets A 150 ml bottle (100 mg/5 ml dosage) of ibuprofen, sold in Greece. Ibuprofen is used primarily to treat fever (including postvaccination fever), mild to moderate pain (including pain relief after surgery), painful menstruation, osteoarthritis, dental pain, headaches, and pain from kidney stones.

  7. Opipramol - Wikipedia

    en.wikipedia.org/wiki/Opipramol

    Opipramol is partially metabolized in the liver to deshydroxyethylopipramol. [3] Metabolism occurs through the CYP2D6 isoenzyme. [3] Its terminal half-life in plasma is 6–11 hours. [3] About 70% is eliminated in urine with 10% unaltered. [3] The remaining portion is eliminated through feces. [3]