Does HEPARIN Cause Suspected product quality issue? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Suspected product quality issue have been filed in association with HEPARIN (Heparin Sodium). This represents 0.1% of all adverse event reports for HEPARIN.
16
Reports of Suspected product quality issue with HEPARIN
0.1%
of all HEPARIN reports
1
Deaths
0
Hospitalizations
How Dangerous Is Suspected product quality issue From HEPARIN?
Of the 16 reports, 1 (6.3%) resulted in death, and 4 (25.0%) were considered life-threatening.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HEPARIN. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does HEPARIN Cause?
Drug ineffective (2,294)
Heparin-induced thrombocytopenia (2,057)
Off label use (1,077)
Thrombocytopenia (781)
Haemorrhage (684)
Pulmonary embolism (652)
Drug hypersensitivity (629)
Thrombosis (603)
Foetal exposure during pregnancy (582)
Anaemia (576)
What Other Drugs Cause Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which HEPARIN Alternatives Have Lower Suspected product quality issue Risk?
HEPARIN vs HEPARIN\SODIUM
HEPARIN vs HEPATITIS B VIRUS VACCINE
HEPARIN vs HERBALS
HEPARIN vs HERBALS\MITRAGYNINE
HEPARIN vs HERBALS\PAULLINIA CUPANA SEED