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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 Incorrect product administration duration (Page 2)

503 drugs have been associated with Incorrect product administration duration in FAERS reports.

Drug Reports Deaths Hosp. Life-Threat.
CANDESARTAN 83 63 75 63
CERTOLIZUMAB PEGOL 80 62 61 61
DELAMANID 80 27 33 5
MOLNUPIRAVIR 80 0 5 0
REGADENOSON 79 0 12 3
CHOLECALCIFEROL 78 63 68 62
PEMBROLIZUMAB 78 5 16 0
RAMIPRIL 78 61 65 72
ERENUMAB-AOOE 77 58 57 57
TOFACITINIB 77 57 60 56
INFLIXIMAB-DYYB 76 0 17 0
TOCILIZUMAB 76 68 68 62
LEFLUNOMIDE 74 69 68 68
RITUXIMAB 74 52 53 56
RITUXIMAB-PVVR 74 5 13 2
CLOFAZIMINE 73 26 27 1
METHYLPREDNISOLONE 73 62 61 62
ALPRAZOLAM 72 0 18 9
AZATHIOPRINE 71 64 66 63
ETANERCEPT 71 56 55 55
FOLIC ACID 70 59 65 58
HUMAN C1-ESTERASE INHIBITOR 70 62 67 61
ABATACEPT 69 55 58 56
HYDROXYCHLOROQUINE 69 60 62 61
LAMOTRIGINE 68 63 64 62
LORATADINE\PSEUDOEPHEDRINE 68 0 0 0
CELECOXIB 67 62 61 61
PANTOPRAZOLE 66 7 15 17
SULFASALAZINE 66 60 59 59
GOLIMUMAB 65 62 61 61
TOPIRAMATE 65 59 59 58
CHLORHEXIDINE 64 63 62 62
DOMPERIDONE 64 64 63 63
ESTRADIOL 64 0 4 0
HISTRELIN 64 0 2 0
HYDROCORTISONE 64 25 28 25
METFORMIN 64 36 47 49
OMADACYCLINE 64 3 22 0
BROMAZEPAM 62 1 27 19
INGENOL MEBUTATE 62 0 2 1
MINOCYCLINE 62 60 60 59
ALENDRONIC ACID 61 58 59 58
DICLOFENAC DIETHYLAMINE 61 54 54 54
ETANERCEPT-SZZS 61 57 56 56
APREMILAST 59 55 54 54
CETIRIZINE\PSEUDOEPHEDRINE 59 52 52 51
GOLD THIOMALATE 59 59 58 58
BOTULINUM TOXIN TYPE A 58 58 57 57
LIDOCAINE 58 0 1 0
ZOLPIDEM 57 0 14 4
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