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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 RIVAROXABAN Cause Incorrect product storage? 22 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Incorrect product storage have been filed in association with RIVAROXABAN (Rivaroxaban). This represents 0.0% of all adverse event reports for RIVAROXABAN.

22
Reports of Incorrect product storage with RIVAROXABAN
0.0%
of all RIVAROXABAN reports
1
Deaths
2
Hospitalizations

How Dangerous Is Incorrect product storage From RIVAROXABAN?

Of the 22 reports, 1 (4.5%) resulted in death, 2 (9.1%) required hospitalization.

Is Incorrect product storage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIVAROXABAN. However, 22 reports have been filed with the FAERS database.

What Other Side Effects Does RIVAROXABAN Cause?

Gastrointestinal haemorrhage (20,041) Haemorrhage (6,571) Epistaxis (5,629) Rectal haemorrhage (4,501) Off label use (4,463) Haematuria (4,387) Upper gastrointestinal haemorrhage (4,247) Cerebrovascular accident (4,111) Anaemia (3,907) Acute kidney injury (3,735)

What Other Drugs Cause Incorrect product storage?

ETANERCEPT (2,149) INSULIN LISPRO (1,114) ABATACEPT (583) TERIPARATIDE (573) ADALIMUMAB (476) GOLIMUMAB (392) INSULIN GLARGINE (341) INSULIN HUMAN (336) USTEKINUMAB (299) ERYTHROPOIETIN (268)

Which RIVAROXABAN Alternatives Have Lower Incorrect product storage Risk?

RIVAROXABAN vs RIVASTIGMINE RIVAROXABAN vs RIVOTRIL RIVAROXABAN vs RIZATRIPTAN RIVAROXABAN vs ROACTEMRA RIVAROXABAN vs ROCURONIUM

Related Pages

RIVAROXABAN Full Profile All Incorrect product storage Reports All Drugs Causing Incorrect product storage RIVAROXABAN Demographics