Does HUMAN RHO IMMUNE GLOBULIN Cause Device issue? 167 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 167 reports of Device issue have been filed in association with HUMAN RHO IMMUNE GLOBULIN (RhoGAM Ultra-Filtered PLUS). This represents 13.8% of all adverse event reports for HUMAN RHO IMMUNE GLOBULIN.
167
Reports of Device issue with HUMAN RHO IMMUNE GLOBULIN
13.8%
of all HUMAN RHO IMMUNE GLOBULIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device issue From HUMAN RHO IMMUNE GLOBULIN?
Of the 167 reports, 1 (0.6%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HUMAN RHO IMMUNE GLOBULIN. However, 167 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)
Syringe issue (154)
Nausea (111)
Treatment failure (110)
Arthralgia (109)
Therapy non-responder (107)
Pain in extremity (104)
Therapeutic product effect decreased (104)
Joint swelling (100)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which HUMAN RHO IMMUNE GLOBULIN Alternatives Have Lower Device issue 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