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
125594671 12559467 1 I 20160623 20160715 20160715 PER US-PFIZER INC-2016316352 PFIZER 34.00 YR M Y 0.00000 20160715 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
125594671 12559467 1 PS DILANTIN PHENYTOIN 1 UNK U 84349 CAPSULE, HARD
125594671 12559467 2 SS VANCOMYCIN HCL VANCOMYCIN HYDROCHLORIDE 1 UNK U 62911
125594671 12559467 3 SS LEVAQUIN LEVOFLOXACIN 1 UNK U 0
125594671 12559467 4 SS TRAZODONE TRAZODONE 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
125594671 12559467 Drug hypersensitivity

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

no results found

Therapies reported

no results found