Does AZD-1222 Cause Intentional product misuse? 300 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 300 reports of Intentional product misuse have been filed in association with AZD-1222. This represents 12.8% of all adverse event reports for AZD-1222.
300
Reports of Intentional product misuse with AZD-1222
12.8%
of all AZD-1222 reports
0
Deaths
76
Hospitalizations
How Dangerous Is Intentional product misuse From AZD-1222?
Of the 300 reports, 76 (25.3%) required hospitalization, and 75 (25.0%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 300 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which AZD-1222 Alternatives Have Lower Intentional product misuse Risk?
AZD-1222 vs AZELAIC ACID
AZD-1222 vs AZELASTINE
AZD-1222 vs AZELASTINE\FLUTICASONE
AZD-1222 vs AZELNIDIPINE
AZD-1222 vs AZILECT