Does ALPHA.1-PROTEINASE INHIBITOR HUMAN Cause Medication error? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Medication error have been filed in association with ALPHA.1-PROTEINASE INHIBITOR HUMAN (GLASSIA). This represents 0.1% of all adverse event reports for ALPHA.1-PROTEINASE INHIBITOR HUMAN.
6
Reports of Medication error with ALPHA.1-PROTEINASE INHIBITOR HUMAN
0.1%
of all ALPHA.1-PROTEINASE INHIBITOR HUMAN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Medication error From ALPHA.1-PROTEINASE INHIBITOR HUMAN?
Of the 6 reports, 1 (16.7%) required hospitalization.
Is Medication error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALPHA.1-PROTEINASE INHIBITOR HUMAN. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does ALPHA.1-PROTEINASE INHIBITOR HUMAN Cause?
Dyspnoea (1,011)
Pneumonia (681)
Fatigue (669)
Headache (631)
Death (456)
Cough (447)
Product dose omission issue (397)
Nausea (385)
Malaise (367)
Dizziness (314)
What Other Drugs Cause Medication error?
ACETAMINOPHEN (1,809)
METHOTREXATE (1,269)
OXYCODONE (1,058)
ADALIMUMAB (954)
DICLOFENAC (915)
TOCILIZUMAB (907)
RITUXIMAB (902)
NAPROXEN (883)
INFLIXIMAB (868)
PREDNISONE (856)
Which ALPHA.1-PROTEINASE INHIBITOR HUMAN Alternatives Have Lower Medication error Risk?
ALPHA.1-PROTEINASE INHIBITOR HUMAN vs ALPRAZOLAM
ALPHA.1-PROTEINASE INHIBITOR HUMAN vs ALPROSTADIL
ALPHA.1-PROTEINASE INHIBITOR HUMAN vs ALTEPLASE
ALPHA.1-PROTEINASE INHIBITOR HUMAN vs ALTERNARIA ALTERNATA
ALPHA.1-PROTEINASE INHIBITOR HUMAN vs ALTHIAZIDE