Does INVESTIGATIONAL PRODUCT Cause Presyncope? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Presyncope have been filed in association with INVESTIGATIONAL PRODUCT. This represents 0.6% of all adverse event reports for INVESTIGATIONAL PRODUCT.
31
Reports of Presyncope with INVESTIGATIONAL PRODUCT
0.6%
of all INVESTIGATIONAL PRODUCT reports
6
Deaths
23
Hospitalizations
How Dangerous Is Presyncope From INVESTIGATIONAL PRODUCT?
Of the 31 reports, 6 (19.4%) resulted in death, 23 (74.2%) required hospitalization, and 6 (19.4%) were considered life-threatening.
Is Presyncope Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INVESTIGATIONAL PRODUCT. However, 31 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 Presyncope?
TREPROSTINIL (585)
BISOPROLOL (485)
LEVONORGESTREL (429)
ADALIMUMAB (420)
AMBRISENTAN (407)
ASPIRIN (370)
TAMSULOSIN (361)
FUROSEMIDE (348)
SERTRALINE (337)
ETANERCEPT (334)
Which INVESTIGATIONAL PRODUCT Alternatives Have Lower Presyncope 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