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  2. Aspirin - Wikipedia

    en.wikipedia.org/wiki/Aspirin

    Aspirin is also used long-term to help prevent further heart attacks, ischaemic strokes, and blood clots in people at high risk. [11] For pain or fever, effects typically begin within 30 minutes. [11] Aspirin works similarly to other NSAIDs but also suppresses the normal functioning of platelets. [11] One common adverse effect is an upset ...

  3. Paracetamol - Wikipedia

    en.wikipedia.org/wiki/Paracetamol

    Paracetamol, [a] or acetaminophen, [b] is a non-opioid analgesic and antipyretic agent used to treat fever and mild to moderate pain. [13] [14] [15] It is a widely available over-the-counter drug sold under various brand names, including Tylenol and Panadol.

  4. Major depressive disorder - Wikipedia

    en.wikipedia.org/wiki/Major_depressive_disorder

    SSRIs are the primary medications prescribed, owing to their relatively mild side-effects, and because they are less toxic in overdose than other antidepressants. [184] People who do not respond to one SSRI can be switched to another antidepressant , and this results in improvement in almost 50% of cases. [ 185 ]

  5. Ibuprofen - Wikipedia

    en.wikipedia.org/wiki/Ibuprofen

    Like aspirin and indomethacin, ibuprofen is a nonselective COX inhibitor, in that it inhibits two isoforms of cyclooxygenase, COX-1 and COX-2. The analgesic , antipyretic , and anti-inflammatory activity of NSAIDs appears to operate mainly through inhibition of COX-2, which decreases the synthesis of prostaglandins involved in mediating ...

  6. Pseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/Pseudoephedrine

    [1] [11] [2] The amount excreted unchanged is dependent on urinary pH similarly to the drug's half-life, as a longer half-life and duration in the body allows more time for the drug to be metabolized. [11] The duration of action of pseudoephedrine, which is dependent on its elimination, is 4 to 12 hours. [1] [12]

  7. Spironolactone - Wikipedia

    en.wikipedia.org/wiki/Spironolactone

    However, only very small amounts of spironolactone and its metabolite canrenone enter breast milk, and the amount received by an infant during breastfeeding (<0.5% of the mother's dose) is considered to be insignificant. [160] A study found that spironolactone was not associated with teratogenicity in the offspring of rats.