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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 Product preparation issue

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176 drugs have been associated with Product preparation issue in FAERS reports.

Drug Reports Deaths Hosp. Life-Threat.
ONABOTULINUMTOXINA 677 0 1 1
COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTEIN C\PROTEIN S HUMAN\PROTHROMBIN 252 2 0 0
HUMAN C1-ESTERASE INHIBITOR 238 1 16 1
SOMATROPIN 200 0 0 0
INCOBOTULINUMTOXINA 174 0 3 0
STIRIPENTOL 129 3 52 1
TESAMORELIN 119 0 2 0
ABATACEPT 115 0 0 0
INFLIXIMAB 101 0 5 0
ABOBOTULINUMTOXINA 91 0 1 2
WATER 82 0 2 0
SODIUM OXYBATE 60 0 5 0
PRABOTULINUMTOXINA-XVFS 56 0 0 0
BELATACEPT 53 0 0 0
CEFUROXIME AXETIL 50 0 1 0
HUMAN IMMUNOGLOBULIN G 45 1 11 0
IPILIMUMAB 45 0 0 0
BELIMUMAB 43 0 3 0
DESMOPRESSIN 43 0 3 0
MEPOLIZUMAB 41 0 2 0
LEUPROLIDE 40 0 0 0
REMDESIVIR 40 0 3 0
COAGULATION FACTOR IX RECOMBINANT HUMAN 39 0 0 0
HUMAN COAGULATION FACTOR VIII/VON WILLEBRAND FACTOR COMPLEX 38 0 2 0
ANTIHEMOPHILIC FACTOR HUMAN 34 1 1 0
NIVOLUMAB 34 1 0 0
NALTREXONE 33 0 1 0
SODIUM 32 0 7 5
DUPILUMAB 31 0 0 0
VEDOLIZUMAB 31 0 4 0
CABOTEGRAVIR 29 0 0 0
ALPHA.1-PROTEINASE INHIBITOR HUMAN 28 0 0 0
ECULIZUMAB 26 1 5 0
FERRIC CARBOXYMALTOSE 26 1 8 6
RAVULIZUMAB-CWVZ 26 2 1 0
TREPROSTINIL 26 1 11 0
IRON SUCROSE 25 0 8 2
MAGNESIUM\POTASSIUM\SODIUM 24 0 0 0
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT 23 0 1 0
EXENATIDE 23 0 1 0
OMALIZUMAB 23 0 6 0
RILPIVIRINE 22 0 0 0
CABOTEGRAVIR\RILPIVIRINE 21 0 0 0
ALGLUCOSIDASE ALFA 19 1 1 0
IRON DEXTRAN 19 0 0 0
RITUXIMAB 19 0 0 0
DUTASTERIDE 18 1 5 0
OCRELIZUMAB 18 0 2 0
POLYETHYLENE GLYCOL 3350 18 0 1 0
SACITUZUMAB GOVITECAN-HZIY 18 0 4 0
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