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  2. Drug intolerance - Wikipedia

    en.wikipedia.org/wiki/Drug_intolerance

    If someone has a very low MTC for a drug, they are likely to experience adverse effects at drug concentrations lower than what it would take to produce the same adverse effects in the general populace; thus, the individual will experience significant toxicity at a dose that is otherwise considered "normal" for the average person.

  3. Contraindication - Wikipedia

    en.wikipedia.org/wiki/Contraindication

    In medicine, a contraindication is a condition (a situation or factor) that serves as a reason not to take a certain medical treatment due to the harm that it would cause the patient. [ 1 ] [ 2 ] Contraindication is the opposite of indication , which is a reason to use a certain treatment.

  4. Tocolytic - Wikipedia

    en.wikipedia.org/wiki/Tocolytic

    Fewer side effects than β 2 agonists. [30] Although not FDA approved in the US, atosiban was developed specifically to delay preterm labor. [31] No current contraindications No maternal adverse effects [32] No adverse effects to the baseline fetal heart rate. No significant difference in neonatal side effect compared to other treatments [32 ...

  5. Suxamethonium chloride - Wikipedia

    en.wikipedia.org/wiki/Suxamethonium_chloride

    Suxamethonium chloride (brand names Scoline and Sucostrin, among others), also known as suxamethonium or succinylcholine, or simply sux in medical abbreviation, [5] is a medication used to cause short-term paralysis as part of general anesthesia. [6]

  6. Procainamide - Wikipedia

    en.wikipedia.org/wiki/Procainamide

    The adverse effects occur even more often if the daily doses are increased. Procainamide may also lead to drug fever and other allergic responses . There is also a chance that drug-induced lupus erythematosus occurs, which at the same time leads to arthralgia , myalgia and pleurisy .

  7. Adverse effect - Wikipedia

    en.wikipedia.org/wiki/Adverse_effect

    Adverse effects, like therapeutic effects of drugs, are a function of dosage or drug levels at the target organs, so they may be avoided or decreased by means of careful and precise pharmacokinetics, the change of drug levels in the organism in function of time after administration. Adverse effects may also be caused by drug interaction. This ...

  8. Ranitidine - Wikipedia

    en.wikipedia.org/wiki/Ranitidine

    Ranitidine has 10% of the affinity that cimetidine has to CYP450, so it causes fewer side effects, but other H 2 blockers famotidine and nizatidine have no CYP450 significant interactions. [ 131 ] Ranitidine was introduced in 1981, and was the world's biggest-selling prescription drug by 1987. [ 132 ]

  9. Isoprenaline - Wikipedia

    en.wikipedia.org/wiki/Isoprenaline

    Side effects of isoprenaline include rapid heart beat, heart palpitations, and arrhythmias, among others. [9] Isoprenaline is a selective agonist of the β-adrenergic receptors, including both the β 1-and β 2-adrenergic receptors. [9] By activating these receptors, it increases heart rate and the force of heart contractions. [10]