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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 Device issue? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Device issue have been filed in association with HEPARIN (Heparin Sodium). This represents 0.1% of all adverse event reports for HEPARIN.

14
Reports of Device issue with HEPARIN
0.1%
of all HEPARIN reports
1
Deaths
3
Hospitalizations

How Dangerous Is Device issue From HEPARIN?

Of the 14 reports, 1 (7.1%) resulted in death, 3 (21.4%) required hospitalization, and 2 (14.3%) were considered life-threatening.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HEPARIN. However, 14 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 Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which HEPARIN Alternatives Have Lower Device 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

Related Pages

HEPARIN Full Profile All Device issue Reports All Drugs Causing Device issue HEPARIN Demographics