Could Multivitamin cause Hepatotoxicity - from FDA reports


Summary

Hepatotoxicity is found among people who take Multivitamin, especially for people who are female, 40-49 old also take medication Tylenol, and have Insomnia . We study 33,007 people who have side effects while taking Multivitamin from FDA. Among them, 15 have Hepatotoxicity. Find out below who they are, when they have Hepatotoxicity and more.

What to expect?

Forecast new symptoms or undetected conditions when you take Multivitamin and have Hepatotoxicity

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Multivitamin

Multivitamin has active ingredients of ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e. It is often used in vitamin supplementation. (latest outcomes from Multivitamin 35,684 users)

Hepatotoxicity

Hepatotoxicity (chemical-driven liver damage) has been reported by people with hiv infection, pain, high blood pressure, preventive health care, rheumatoid arthritis (latest reports from 8,173 Hepatotoxicity patients).

On Dec, 06, 2016

33,007 people reported to have side effects when taking Multivitamin.
Among them, 15 people (0.05%) have Hepatotoxicity


Number of reports submitted per year:

Could Multivitamin cause Hepatotoxicity?

Gender of people who have Hepatotoxicity when taking Multivitamin *:

  • female: 66.67 %
  • male: 33.33 %

Age of people who have Hepatotoxicity when taking Multivitamin *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 6.67 %
  • 40-49: 60.0 %
  • 50-59: 6.67 %
  • 60+: 26.67 %

Top co-used drugs for these people *:

  • Tylenol (6 people, 40.00%)
  • Zetia (5 people, 33.33%)
  • Diovan (5 people, 33.33%)
  • Verelan (4 people, 26.67%)
  • Lorazepam (3 people, 20.00%)

Forecasts by ePatient.care (We will alert you to new symptoms or undetected conditions when you take Multivitamin, learn more )

Potential co-existing conditions

  • Insomnia (4 people, 26.67%)
  • Pain (3 people, 20.00%)
  • Congenital Cystic Kidney Disease (3 people, 20.00%)
  • Rosacea (2 people, 13.33%)
  • Nausea (2 people, 13.33%)

Potential co-existing symptoms

  • Blood Bilirubin Increased (5 people, 33.33%)
  • Aspartate Aminotransferase Increased (5 people, 33.33%)
  • Umbilical Hernia (4 people, 26.67%)
  • Liver Function Test Abnormal (4 people, 26.67%)
  • Appetite - Decreased (4 people, 26.67%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

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