Does HUMAN RHO IMMUNE GLOBULIN Cause Device breakage? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device breakage have been filed in association with HUMAN RHO IMMUNE GLOBULIN (RhoGAM Ultra-Filtered PLUS). This represents 0.8% of all adverse event reports for HUMAN RHO IMMUNE GLOBULIN.
9
Reports of Device breakage with HUMAN RHO IMMUNE GLOBULIN
0.8%
of all HUMAN RHO IMMUNE GLOBULIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device breakage From HUMAN RHO IMMUNE GLOBULIN?
Of the 9 reports.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HUMAN RHO IMMUNE GLOBULIN. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does HUMAN RHO IMMUNE GLOBULIN Cause?
No adverse event (238)
Drug ineffective (201)
Device issue (167)
Syringe issue (154)
Nausea (111)
Treatment failure (110)
Arthralgia (109)
Therapy non-responder (107)
Pain in extremity (104)
Therapeutic product effect decreased (104)
What Other Drugs Cause Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which HUMAN RHO IMMUNE GLOBULIN Alternatives Have Lower Device breakage Risk?
HUMAN RHO IMMUNE GLOBULIN vs HUMIRA
HUMAN RHO IMMUNE GLOBULIN vs HUMIRA PEN
HUMAN RHO IMMUNE GLOBULIN vs HYALURONATE
HUMAN RHO IMMUNE GLOBULIN vs HYALURONIC ACID
HUMAN RHO IMMUNE GLOBULIN vs HYALURONIC ACID\LIDOCAINE