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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 BUROSUMAB Cause Product storage error? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product storage error have been filed in association with BUROSUMAB (CRYSVITA). This represents 2.1% of all adverse event reports for BUROSUMAB.

14
Reports of Product storage error with BUROSUMAB
2.1%
of all BUROSUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product storage error From BUROSUMAB?

Of the 14 reports, 1 (7.1%) required hospitalization.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BUROSUMAB. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does BUROSUMAB Cause?

Product dose omission issue (124) Pain (69) Inappropriate schedule of product administration (64) Arthralgia (59) Therapy interrupted (57) Blood phosphorus decreased (53) Pain in extremity (50) Restless legs syndrome (49) Back pain (35) Fatigue (34)

What Other Drugs Cause Product storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which BUROSUMAB Alternatives Have Lower Product storage error Risk?

BUROSUMAB vs BUROSUMAB-TWZA BUROSUMAB vs BUSPIRONE BUROSUMAB vs BUSULFAN BUROSUMAB vs BUSULFEX BUROSUMAB vs BUTALBITAL

Related Pages

BUROSUMAB Full Profile All Product storage error Reports All Drugs Causing Product storage error BUROSUMAB Demographics