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
127674791 12767479 1 I 0 20160921 20160921 DIR US-FDA-351148 FDA-CTU 62.00 YR F N 99.00000 KG 20160921 Y 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
127674791 12767479 1 PS VENLAFAXINE HCL ER 225 MG PFIZER VENLAFAXINE HYDROCHLORIDE 1 Oral N D 16940P1 99 90 DF QD
127674791 12767479 2 C ALPRAZOLM 2 0
127674791 12767479 4 C FENOFIBRATE. FENOFIBRATE 1 0
127674791 12767479 6 C LISINOPRIL. LISINOPRIL 1 0
127674791 12767479 8 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
127674791 12767479 10 C PRAVASTATIN. PRAVASTATIN 1 0
127674791 12767479 12 C FISH OIL FISH OIL 1 0
127674791 12767479 14 C ASPIRIN. ASPIRIN 1 0
127674791 12767479 16 C VITAMIN D3 CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127674791 12767479 1 Major depression

Outcome of event

Event ID CASEID OUTC COD
127674791 12767479 OT
127674791 12767479 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127674791 12767479 Depression
127674791 12767479 Drug withdrawal syndrome
127674791 12767479 Product solubility abnormal

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

no results found

Therapies reported

no results found