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  2. Doxylamine - Wikipedia

    en.wikipedia.org/wiki/Doxylamine

    Side effects of doxylamine include dizziness, drowsiness, and dry mouth, among others. [4] Doxylamine is a potent anticholinergic and has a side-effect profile common to such drugs, including blurred vision, dry mouth, constipation, muscle incoordination, urinary retention, mental confusion, and delirium. [18] [7]

  3. H1 antagonist - Wikipedia

    en.wikipedia.org/wiki/H1_antagonist

    7.5–15 mg 2 hours 20–40 hours CYP2D6, others No Quetiapine e: 25–200 mg 1.5 hours 7 hours d: CYP3A4 No (at low doses) Footnotes: a = For sleep/sedation. b = In adults. c Active metabolite nordoxepin half-life is 31 hours. d Active metabolite norquetiapine half-life is 9–12 hours. e Not recommended per literature reviews.

  4. Antihistamine - Wikipedia

    en.wikipedia.org/wiki/Antihistamine

    Antihistamines are drugs which treat allergic rhinitis, common cold, influenza, and other allergies. [1] Typically, people take antihistamines as an inexpensive, generic (not patented) drug that can be bought without a prescription and provides relief from nasal congestion, sneezing, or hives caused by pollen, dust mites, or animal allergy with few side effects. [1]

  5. Levmetamfetamine - Wikipedia

    en.wikipedia.org/wiki/Levmetamfetamine

    [2] [3] However, higher doses of levmetamfetamine, for instance 0.25 to 0.5 mg/kg (mean doses of ~18–37 mg) intravenously, have been reported to produce significant pharmacological effects, including increased heart rate and blood pressure, increased respiration rate, and subjective effects like intoxication and drug liking.

  6. List of herbs with known adverse effects - Wikipedia

    en.wikipedia.org/wiki/List_of_herbs_with_known...

    Very rarely Stevens–Johnson syndrome, liver damage, severe allergy has been reported [17] May lower blood sugar excessively in combination with diabetes medication. [17] Contains a chemical linked to possible birth defects. [17]

  7. Chlorphenamine - Wikipedia

    en.wikipedia.org/wiki/Chlorphenamine

    [24] [25] The smaller the K d value, the greater the binding affinity of the ligand for its target. In addition to acting as an inverse agonist at the H 1 receptor, chlorphenamine has been found to act as a serotonin reuptake inhibitor (K d = 15.2 nM for the serotonin transporter ).