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  2. Lamotrigine - Wikipedia

    en.wikipedia.org/wiki/Lamotrigine

    The side-effects profile varies for different patient populations. [50] Overall adverse effects in treatment are similar between men, women, geriatric, pediatric, and racial groups. [5] Lamotrigine has been associated with a decrease in white blood cell count . [53] Lamotrigine does not prolong QT/QTc in TQT studies in healthy subjects. [54]

  3. Tamsulosin - Wikipedia

    en.wikipedia.org/wiki/Tamsulosin

    Common side effects include dizziness, headache, insomnia, nausea, blurry vision, and sexual problems. [9] [6] Other side effects may include feeling lightheaded with standing due to changes in blood pressure, and angioedema. [9] Tamsulosin is an alpha blocker and works by relaxing muscles in the prostate. [10]

  4. Adderall - Wikipedia

    en.wikipedia.org/wiki/Adderall

    Adderall and Mydayis [11] are trade names [note 2] for a combination drug containing four salts of amphetamine.The mixture is composed of equal parts racemic amphetamine and dextroamphetamine, which produces a (3:1) ratio between dextroamphetamine and levoamphetamine, the two enantiomers of amphetamine. [13]

  5. Tetryzoline - Wikipedia

    en.wikipedia.org/wiki/Tetryzoline

    In a healthy person, the biological half-life of tetryzoline is approximately 6 hours, and it is excreted in urine, chemically unchanged, at least in part. In one study, 10 people were given two drops of 0.5 mg/mL of tetryzoline eye drops (0.025–0.05 mg) at 0 hrs, 4 hrs, 8 hrs, and 12 hrs.

  6. Biperiden - Wikipedia

    en.wikipedia.org/wiki/Biperiden

    Common side effects include blurred vision, dry mouth, sleepiness, constipation, and confusion. [2] It should not be used in people with a bowel obstruction or glaucoma. [2] It is unclear if use in pregnancy or breastfeeding is safe. [4] Biperiden is in the anticholinergic family of medication. [2]

  7. Therapeutic index - Wikipedia

    en.wikipedia.org/wiki/Therapeutic_index

    It is desirous for the value of LD 50 to be as large as possible, to decrease risk of lethal effects and increase the therapeutic window. In the above formula, TI safety increases as the difference between LD 50 and ED 50 increases—hence, a higher safety-based therapeutic index indicates a larger therapeutic window, and vice versa.