The Safety Rates Drug Report

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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
121564602 12156460 2 F 20160712 20160307 20160718 PER US-PFIZER INC-2016137157 PFIZER 0.00 F Y 0.00000 20160718 OT 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
121564602 12156460 1 PS CLINDAMYCIN HCL CLINDAMYCIN HYDROCHLORIDE 1 UNK U 50162 CAPSULE, HARD
121564602 12156460 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U 77245
121564602 12156460 3 SS CEFDINIR. CEFDINIR 1 UNK U 0
121564602 12156460 4 SS MACRODANTIN NITROFURANTOIN 1 UNK U 0
121564602 12156460 5 SS ASPIRIN. ASPIRIN 1 UNK U 0
121564602 12156460 6 SS DARVOCET ACETAMINOPHENPROPOXYPHENE HYDROCHLORIDE 1 UNK U 0
121564602 12156460 7 SS PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 UNK U 0
121564602 12156460 8 SS ULTRAM TRAMADOL HYDROCHLORIDE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121564602 12156460 Drug hypersensitivity
121564602 12156460 Rash
121564602 12156460 Urticaria

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

no results found

Therapies reported

no results found