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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AZD-1222 Cause Medication error? 148 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 148 reports of Medication error have been filed in association with AZD-1222. This represents 6.3% of all adverse event reports for AZD-1222.

148
Reports of Medication error with AZD-1222
6.3%
of all AZD-1222 reports
0
Deaths
33
Hospitalizations

How Dangerous Is Medication error From AZD-1222?

Of the 148 reports, 33 (22.3%) required hospitalization, and 3 (2.0%) were considered life-threatening.

Is Medication error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 148 reports have been filed with the FAERS database.

What Other Side Effects Does AZD-1222 Cause?

Headache (838) Fatigue (784) Pyrexia (735) Pain (579) Covid-19 (515) Arthralgia (508) Nausea (494) Palpitations (485) Dyspnoea (472) Abdominal discomfort (467)

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 AZD-1222 Alternatives Have Lower Medication error Risk?

AZD-1222 vs AZELAIC ACID AZD-1222 vs AZELASTINE AZD-1222 vs AZELASTINE\FLUTICASONE AZD-1222 vs AZELNIDIPINE AZD-1222 vs AZILECT

Related Pages

AZD-1222 Full Profile All Medication error Reports All Drugs Causing Medication error AZD-1222 Demographics