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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.

All Drugs Associated with Wrong technique in product usage process (Page 13)

1,196 drugs have been associated with Wrong technique in product usage process in FAERS reports.

Drug Reports Deaths Hosp. Life-Threat.
ABROCITINIB 23 0 2 0
ACETAMINOPHEN\IBUPROFEN 23 0 0 0
AZATHIOPRINE 23 0 4 2
EMTRICITABINE\TENOFOVIR DISOPROXIL 23 1 0 0
HYDROCHLOROTHIAZIDE\LISINOPRIL 23 0 0 2
INDACATEROL 23 3 13 1
LOTEPREDNOL ETABONATE 23 0 0 0
SALMETEROL 23 0 0 0
TACROLIMUS\TACROLIMUS ANHYDROUS 23 0 4 0
TAMOXIFEN 23 1 5 0
TIZANIDINE 23 0 3 0
BEVACIZUMAB-AWWB 22 0 0 0
BIMEKIZUMAB 22 0 5 0
BOSUTINIB 22 0 3 1
COLLAGENASE CLOSTRIDIUM HISTOLYTICUM-AAES 22 0 0 0
DONEPEZIL 22 0 6 1
DORZOLAMIDE 22 0 0 0
ERLOTINIB 22 3 2 0
GLYCOPYRROLATE\INDACATEROL 22 2 4 4
MOXONIDINE 22 0 6 0
PACLITAXEL 22 0 1 1
SECNIDAZOLE 22 0 0 0
SOFOSBUVIR 22 1 6 0
ADAPALENE 21 0 0 0
AMPHETAMINE 21 0 5 0
APALUTAMIDE 21 0 3 0
CANDESARTAN CILEXETIL 21 1 4 0
CARBOXYMETHYLCELLULOSE 21 1 2 0
CILGAVIMAB\TIXAGEVIMAB 21 1 0 0
DIAMORPHINE 21 2 5 1
ETELCALCETIDE 21 0 0 0
LABETALOL\LABETALOL 21 0 0 0
PAZOPANIB 21 6 8 1
PENICILLIN 21 0 5 0
RIZATRIPTAN 21 1 0 0
SOTALOL 21 0 5 1
TENAPANOR 21 0 4 0
TETRAZEPAM 21 0 0 0
TUBERCULIN PURIFIED PROTEIN DERIVATIVE 21 0 0 0
VEMURAFENIB 21 2 0 0
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT 20 0 6 1
BOSENTAN 20 1 6 0
BROMAZEPAM 20 0 3 1
CALCIUM\MAGNESIUM\POTASSIUM\SODIUM\SODIUM\SODIUM 20 0 1 0
CAPLACIZUMAB-YHDP 20 0 2 0
CEFUROXIME AXETIL 20 0 2 1
CICLESONIDE 20 0 17 0
DOXEPIN 20 0 0 0
ENTECAVIR 20 0 8 1
FENFLURAMINE 20 0 7 0
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