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
126765972 12676597 2 F 20160819 20160823 20160824 PER US-PFIZER INC-2016397131 PFIZER 55.00 YR F Y 0.00000 20160824 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
126765972 12676597 1 PS CLINDAMYCIN HCL CLINDAMYCIN HYDROCHLORIDE 1 UNK U 50162 CAPSULE, HARD
126765972 12676597 2 SS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 UNK U 50670
126765972 12676597 3 SS ERYTHROMYCIN. ERYTHROMYCIN 1 UNK U 50609
126765972 12676597 4 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U 77245
126765972 12676597 5 SS AMANTADINE HCL AMANTADINE HYDROCHLORIDE 1 UNK U 0
126765972 12676597 6 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 UNK U 0
126765972 12676597 7 SS CODEINE CODEINE 1 UNK U 0
126765972 12676597 8 SS KEFLEX CEPHALEXIN 1 UNK U 0
126765972 12676597 9 SS MACRODANTIN NITROFURANTOIN 1 UNK U 0
126765972 12676597 10 SS OPANA OXYMORPHONE 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
126765972 12676597 Drug hypersensitivity
126765972 12676597 Rash

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

no results found

Therapies reported

no results found