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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 Rheumatoid arthritis? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Rheumatoid arthritis have been filed in association with AZD-1222. This represents 0.9% of all adverse event reports for AZD-1222.

21
Reports of Rheumatoid arthritis with AZD-1222
0.9%
of all AZD-1222 reports
0
Deaths
5
Hospitalizations

How Dangerous Is Rheumatoid arthritis From AZD-1222?

Of the 21 reports, 5 (23.8%) required hospitalization.

Is Rheumatoid arthritis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 21 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 Rheumatoid arthritis?

ETANERCEPT (33,166) ADALIMUMAB (29,817) METHOTREXATE (29,254) ABATACEPT (21,898) LEFLUNOMIDE (20,886) TOCILIZUMAB (20,652) HYDROXYCHLOROQUINE (20,110) RITUXIMAB (19,850) CERTOLIZUMAB PEGOL (17,782) INFLIXIMAB (16,251)

Which AZD-1222 Alternatives Have Lower Rheumatoid arthritis 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 Rheumatoid arthritis Reports All Drugs Causing Rheumatoid arthritis AZD-1222 Demographics