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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 Hyperhidrosis? 368 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 368 reports of Hyperhidrosis have been filed in association with AZD-1222. This represents 15.7% of all adverse event reports for AZD-1222.

368
Reports of Hyperhidrosis with AZD-1222
15.7%
of all AZD-1222 reports
0
Deaths
81
Hospitalizations

How Dangerous Is Hyperhidrosis From AZD-1222?

Of the 368 reports, 81 (22.0%) required hospitalization, and 82 (22.3%) were considered life-threatening.

Is Hyperhidrosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 368 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 Hyperhidrosis?

DULOXETINE (4,101) ADALIMUMAB (2,745) SODIUM (2,444) VENLAFAXINE (1,932) LEVOTHYROXINE (1,856) ACETAMINOPHEN (1,578) ETANERCEPT (1,521) MORPHINE (1,438) GABAPENTIN (1,408) PREGABALIN (1,385)

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