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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 DIDANOSINE Cause Hepatic function abnormal? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Hepatic function abnormal have been filed in association with DIDANOSINE. This represents 0.6% of all adverse event reports for DIDANOSINE.

12
Reports of Hepatic function abnormal with DIDANOSINE
0.6%
of all DIDANOSINE reports
1
Deaths
3
Hospitalizations

How Dangerous Is Hepatic function abnormal From DIDANOSINE?

Of the 12 reports, 1 (8.3%) resulted in death, 3 (25.0%) required hospitalization, and 1 (8.3%) were considered life-threatening.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DIDANOSINE. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does DIDANOSINE Cause?

Foetal exposure during pregnancy (472) Lipodystrophy acquired (216) Eyelid ptosis (191) Drug resistance (189) Virologic failure (187) Mitochondrial toxicity (174) Viral mutation identified (171) Diplopia (170) Treatment failure (170) Pathogen resistance (135)

What Other Drugs Cause Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which DIDANOSINE Alternatives Have Lower Hepatic function abnormal Risk?

DIDANOSINE vs DIENOGEST DIDANOSINE vs DIENOGEST\ESTRADIOL DIDANOSINE vs DIENOGEST\ETHINYL ESTRADIOL DIDANOSINE vs DIETARY SUPPLEMENT DIDANOSINE vs DIETARY SUPPLEMENT\HERBALS

Related Pages

DIDANOSINE Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal DIDANOSINE Demographics