The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
95568416 9556841 6 F 20160808 20130926 20160815 PER US-PFIZER INC-2013275408 PFIZER 62.00 YR F Y 0.00000 20160815 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
95568416 9556841 1 PS CELEBREX CELECOXIB 1 UNK U 20998 CAPSULE, HARD
95568416 9556841 2 SS DETROL LA TOLTERODINE TARTRATE 1 Oral 4 MG, 1X/DAY U 21228 4 MG MODIFIED-RELEASE CAPSULE, SOFT QD
95568416 9556841 3 SS TRAMADOL HCL TRAMADOL HYDROCHLORIDE 1 UNK U 0
95568416 9556841 4 SS SILVER SULFADIAZENE SILVER SULFADIAZINE 1 UNK U 17381 CREAM
95568416 9556841 5 SS DESYREL TRAZODONE HYDROCHLORIDE 1 UNK U 0
95568416 9556841 6 SS ULTRAM TRAMADOL HYDROCHLORIDE 1 UNK U 0
95568416 9556841 7 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 UNK U 0
95568416 9556841 8 SS PHENOBARB PHENOBARBITAL SODIUM 1 UNK U 0
95568416 9556841 9 SS NSA UNSPECIFIED INGREDIENT 1 UNK U 0
95568416 9556841 10 SS IODINE. IODINE 1 UNK U 0
95568416 9556841 11 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
95568416 9556841 12 C SYNTHROID LEVOTHYROXINE SODIUM 1 UNK 0
95568416 9556841 13 C DULOXETINE. DULOXETINE 1 UNK 0
95568416 9556841 14 C DOXEPIN HCL DOXEPIN HYDROCHLORIDE 1 UNK 0
95568416 9556841 15 C TIZANIDINE. TIZANIDINE 1 UNK 0
95568416 9556841 16 C VALSARTAN. VALSARTAN 1 UNK 0
95568416 9556841 17 C AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 UNK 0
95568416 9556841 18 C LASIX FUROSEMIDE 1 UNK, AS NEEDED 0
95568416 9556841 19 C PRENATAL VITAMINS /02014401/ VITAMINS 1 UNK 0
95568416 9556841 20 C VITAMIN D3 CHOLECALCIFEROL 1 2000 IU, UNK 0 2000 IU
95568416 9556841 21 C HYDROCODONE HYDROCODONE 1 UNK, AS NEEDED 0
95568416 9556841 22 C GABAPENTIN. GABAPENTIN 1 UNK 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
95568416 9556841 Drug hypersensitivity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found