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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 INVESTIGATIONAL PRODUCT Cause Left ventricular dysfunction? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Left ventricular dysfunction have been filed in association with INVESTIGATIONAL PRODUCT. This represents 0.2% of all adverse event reports for INVESTIGATIONAL PRODUCT.

9
Reports of Left ventricular dysfunction with INVESTIGATIONAL PRODUCT
0.2%
of all INVESTIGATIONAL PRODUCT reports
0
Deaths
6
Hospitalizations

How Dangerous Is Left ventricular dysfunction From INVESTIGATIONAL PRODUCT?

Of the 9 reports, 6 (66.7%) required hospitalization, and 1 (11.1%) were considered life-threatening.

Is Left ventricular dysfunction Listed in the Official Label?

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

What Other Side Effects Does INVESTIGATIONAL PRODUCT Cause?

Febrile neutropenia (241) Pneumonia (229) Acute kidney injury (198) Pyrexia (189) Anaemia (176) Diarrhoea (170) Sepsis (168) Dyspnoea (156) Nausea (134) Hypotension (130)

What Other Drugs Cause Left ventricular dysfunction?

DOXORUBICIN (430) CYCLOPHOSPHAMIDE (426) TRASTUZUMAB (401) CLOZAPINE (231) SACUBITRIL\VALSARTAN (231) BISOPROLOL (225) PERTUZUMAB (207) RITUXIMAB (202) DOCETAXEL (199) VINCRISTINE (193)

Which INVESTIGATIONAL PRODUCT Alternatives Have Lower Left ventricular dysfunction Risk?

INVESTIGATIONAL PRODUCT vs INVOKANA INVESTIGATIONAL PRODUCT vs IOBENGUANE I-131 INVESTIGATIONAL PRODUCT vs IOBITRIDOL INVESTIGATIONAL PRODUCT vs IODINE INVESTIGATIONAL PRODUCT vs IODINE\IOFLUPANE I-123

Related Pages

INVESTIGATIONAL PRODUCT Full Profile All Left ventricular dysfunction Reports All Drugs Causing Left ventricular dysfunction INVESTIGATIONAL PRODUCT Demographics