Does ADAMTS13, RECOMBINANT-KRHN Cause Incorrect dose administered? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Incorrect dose administered have been filed in association with ADAMTS13, RECOMBINANT-KRHN. This represents 7.4% of all adverse event reports for ADAMTS13, RECOMBINANT-KRHN.
5
Reports of Incorrect dose administered with ADAMTS13, RECOMBINANT-KRHN
7.4%
of all ADAMTS13, RECOMBINANT-KRHN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect dose administered From ADAMTS13, RECOMBINANT-KRHN?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Incorrect dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADAMTS13, RECOMBINANT-KRHN. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does ADAMTS13, RECOMBINANT-KRHN Cause?
Pregnancy (9)
No adverse event (7)
Thrombotic thrombocytopenic purpura (6)
Abortion spontaneous (5)
Headache (5)
What Other Drugs Cause Incorrect dose administered?
TIRZEPATIDE (23,301)
ADALIMUMAB (14,000)
DUPILUMAB (9,907)
RANITIDINE (9,337)
INSULIN LISPRO (8,318)
ACETAMINOPHEN (5,316)
DULAGLUTIDE (5,207)
SECUKINUMAB (4,524)
INSULIN GLARGINE (3,070)
SOMATROPIN (2,772)