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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 UNSPECIFIED INGREDIENT Cause Cholecystitis chronic? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Cholecystitis chronic have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.0% of all adverse event reports for UNSPECIFIED INGREDIENT.

9
Reports of Cholecystitis chronic with UNSPECIFIED INGREDIENT
0.0%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
9
Hospitalizations

How Dangerous Is Cholecystitis chronic From UNSPECIFIED INGREDIENT?

Of the 9 reports, 9 (100.0%) required hospitalization.

Is Cholecystitis chronic Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?

Death (2,090) Off label use (1,306) Drug ineffective (1,227) Completed suicide (1,190) Nausea (1,041) Fatigue (1,020) Dyspnoea (934) Pneumonia (903) Asthenia (894) Vomiting (877)

What Other Drugs Cause Cholecystitis chronic?

YAZ (414) YASMIN (387) OCELLA (161) OLMESARTAN MEDOXOMIL (137) HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL (112) DROSPIRENONE\ETHINYL ESTRADIOL (45) SEMAGLUTIDE (30) SITAGLIPTIN (28) ADALIMUMAB (24) GIANVI (21)

Which UNSPECIFIED INGREDIENT Alternatives Have Lower Cholecystitis chronic Risk?

UNSPECIFIED INGREDIENT vs UPADACITINIB UNSPECIFIED INGREDIENT vs URAPIDIL UNSPECIFIED INGREDIENT vs UREA UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE UNSPECIFIED INGREDIENT vs UROFOLLITROPIN

Related Pages

UNSPECIFIED INGREDIENT Full Profile All Cholecystitis chronic Reports All Drugs Causing Cholecystitis chronic UNSPECIFIED INGREDIENT Demographics