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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 Syncope? 83 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 83 reports of Syncope have been filed in association with INVESTIGATIONAL PRODUCT. This represents 1.5% of all adverse event reports for INVESTIGATIONAL PRODUCT.

83
Reports of Syncope with INVESTIGATIONAL PRODUCT
1.5%
of all INVESTIGATIONAL PRODUCT reports
12
Deaths
77
Hospitalizations

How Dangerous Is Syncope From INVESTIGATIONAL PRODUCT?

Of the 83 reports, 12 (14.5%) resulted in death, 77 (92.8%) required hospitalization, and 8 (9.6%) were considered life-threatening.

Is Syncope Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for INVESTIGATIONAL PRODUCT. However, 83 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 Syncope?

AMBRISENTAN (2,140) TREPROSTINIL (1,908) ADALIMUMAB (1,795) FUROSEMIDE (1,431) LENALIDOMIDE (1,280) BISOPROLOL (1,279) METOPROLOL (1,251) AMLODIPINE (1,224) ASPIRIN (1,193) SACUBITRIL\VALSARTAN (1,163)

Which INVESTIGATIONAL PRODUCT Alternatives Have Lower Syncope 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 Syncope Reports All Drugs Causing Syncope INVESTIGATIONAL PRODUCT Demographics