Does RITUXIMAB Cause Maternal exposure timing unspecified? 402 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 402 reports of Maternal exposure timing unspecified have been filed in association with RITUXIMAB (Rituxan). This represents 0.2% of all adverse event reports for RITUXIMAB.
402
Reports of Maternal exposure timing unspecified with RITUXIMAB
0.2%
of all RITUXIMAB reports
242
Deaths
274
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From RITUXIMAB?
Of the 402 reports, 242 (60.2%) resulted in death, 274 (68.2%) required hospitalization, and 239 (59.5%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB. However, 402 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB Cause?
Off label use (39,751)
Drug ineffective (32,186)
Rheumatoid arthritis (19,850)
Pain (16,675)
Fatigue (15,602)
Arthralgia (12,529)
Rash (12,102)
Drug intolerance (11,876)
Infusion related reaction (11,871)
Joint swelling (11,170)
What Other Drugs Cause Maternal exposure timing unspecified?
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
OXYCODONE (300)
Which RITUXIMAB Alternatives Have Lower Maternal exposure timing unspecified Risk?
RITUXIMAB vs RITUXIMAB-ABBS
RITUXIMAB vs RITUXIMAB-ARRX
RITUXIMAB vs RITUXIMAB-PVVR
RITUXIMAB vs RIVAROXABAN
RITUXIMAB vs RIVASTIGMINE