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
125927351 12592735 1 I 20160718 20160726 20160726 PER US-PFIZER INC-2016352144 PFIZER 0.00 Y 0.00000 20160726 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
125927351 12592735 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U 77245
125927351 12592735 2 SS CLINDAMYCIN HCL CLINDAMYCIN HYDROCHLORIDE 1 UNK U 50162 CAPSULE, HARD
125927351 12592735 3 SS LAMISIL TERBINAFINE HYDROCHLORIDE 1 UNK U 0
125927351 12592735 4 SS LORTAB ACETAMINOPHENHYDROCODONE BITARTRATE 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
125927351 12592735 Drug hypersensitivity

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

no results found

Therapies reported

no results found