Does AZD-1222 Cause Dysgeusia? 123 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 123 reports of Dysgeusia have been filed in association with AZD-1222. This represents 5.3% of all adverse event reports for AZD-1222.
123
Reports of Dysgeusia with AZD-1222
5.3%
of all AZD-1222 reports
0
Deaths
10
Hospitalizations
How Dangerous Is Dysgeusia From AZD-1222?
Of the 123 reports, 10 (8.1%) required hospitalization, and 3 (2.4%) were considered life-threatening.
Is Dysgeusia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 123 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 Dysgeusia?
NIRMATRELVIR\RITONAVIR (7,381)
SUNITINIB MALATE (1,226)
SODIUM (1,216)
LENALIDOMIDE (1,180)
LIFITEGRAST (1,067)
CABOZANTINIB S-MALATE (777)
CLARITHROMYCIN (717)
VISMODEGIB (706)
ADALIMUMAB (674)
PALBOCICLIB (620)
Which AZD-1222 Alternatives Have Lower Dysgeusia Risk?
AZD-1222 vs AZELAIC ACID
AZD-1222 vs AZELASTINE
AZD-1222 vs AZELASTINE\FLUTICASONE
AZD-1222 vs AZELNIDIPINE
AZD-1222 vs AZILECT