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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 BEMIPARIN Cause Product dose omission issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product dose omission issue have been filed in association with BEMIPARIN. This represents 6.8% of all adverse event reports for BEMIPARIN.

5
Reports of Product dose omission issue with BEMIPARIN
6.8%
of all BEMIPARIN reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product dose omission issue From BEMIPARIN?

Of the 5 reports, 5 (100.0%) required hospitalization.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BEMIPARIN. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does BEMIPARIN Cause?

Pruritus (8) Rash maculo-papular (8) Hepatic cytolysis (7) Hepatitis (7) Drug intolerance (6) Memory impairment (6) Respiratory tract infection (6) Acute kidney injury (5) Foetal exposure during pregnancy (5)

What Other Drugs Cause Product dose omission issue?

DUPILUMAB (18,189) USTEKINUMAB (9,405) GUSELKUMAB (9,267) LENALIDOMIDE (8,145) MEPOLIZUMAB (5,873) TOFACITINIB (5,646) VOXELOTOR (5,122) BELIMUMAB (4,671) SECUKINUMAB (4,572) APREMILAST (4,460)

Related Pages

BEMIPARIN Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue BEMIPARIN Demographics