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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does HUMAN ROTAVIRUS A Cause Transaminases increased? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Transaminases increased have been filed in association with HUMAN ROTAVIRUS A. This represents 29.6% of all adverse event reports for HUMAN ROTAVIRUS A.

8
Reports of Transaminases increased with HUMAN ROTAVIRUS A
29.6%
of all HUMAN ROTAVIRUS A reports
0
Deaths
0
Hospitalizations

How Dangerous Is Transaminases increased From HUMAN ROTAVIRUS A?

Of the 8 reports.

Is Transaminases increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HUMAN ROTAVIRUS A. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does HUMAN ROTAVIRUS A Cause?

Foetal exposure during pregnancy (13) Cholestasis (8) Hypovitaminosis (8) Liver injury (8) Diarrhoea (5) Pyrexia (5)

What Other Drugs Cause Transaminases increased?

METHOTREXATE (1,236) ACETAMINOPHEN (929) ATORVASTATIN (472) RITUXIMAB (448) CYCLOPHOSPHAMIDE (401) PREDNISONE (362) ADALIMUMAB (340) PACLITAXEL (333) ROSUVASTATIN (324) CARBOPLATIN (319)

Related Pages

HUMAN ROTAVIRUS A Full Profile All Transaminases increased Reports All Drugs Causing Transaminases increased HUMAN ROTAVIRUS A Demographics