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
125462812 12546281 2 F 20160708 20160711 20160712 PER US-PFIZER INC-2016328363 PFIZER 0.00 F Y 0.00000 20160712 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
125462812 12546281 1 PS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 UNK U 20699 TABLET
125462812 12546281 2 SS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 UNK U 50670
125462812 12546281 3 SS CODEINE CODEINE 1 UNK U 0
125462812 12546281 4 SS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 UNK U 0
125462812 12546281 5 SS ZESTRIL LISINOPRIL 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
125462812 12546281 Drug hypersensitivity

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

no results found

Therapies reported

no results found