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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 HEPARIN Cause Product administration error? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Product administration error have been filed in association with HEPARIN (Heparin Sodium). This represents 0.2% of all adverse event reports for HEPARIN.

31
Reports of Product administration error with HEPARIN
0.2%
of all HEPARIN reports
7
Deaths
14
Hospitalizations

How Dangerous Is Product administration error From HEPARIN?

Of the 31 reports, 7 (22.6%) resulted in death, 14 (45.2%) required hospitalization, and 11 (35.5%) were considered life-threatening.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HEPARIN. However, 31 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 Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which HEPARIN Alternatives Have Lower Product administration error Risk?

HEPARIN vs HEPARIN\SODIUM HEPARIN vs HEPATITIS B VIRUS VACCINE HEPARIN vs HERBALS HEPARIN vs HERBALS\MITRAGYNINE HEPARIN vs HERBALS\PAULLINIA CUPANA SEED

Related Pages

HEPARIN Full Profile All Product administration error Reports All Drugs Causing Product administration error HEPARIN Demographics