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
125937911 12593791 1 I 201502 20160719 20160726 20160726 EXP GB-MHRA-EYC 00142439 GB-PFIZER INC-2016353841 PFIZER 57.00 YR M Y 80.73000 KG 20160726 CN GB GB

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
125937911 12593791 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 37.5 MG, 2X/DAY 20699 37.5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125937911 12593791 1 Depression

Outcome of event

Event ID CASEID OUTC COD
125937911 12593791 OT
125937911 12593791 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125937911 12593791 Balance disorder
125937911 12593791 Breath sounds abnormal
125937911 12593791 Condition aggravated
125937911 12593791 Drug withdrawal headache
125937911 12593791 Dry mouth
125937911 12593791 Dysgeusia
125937911 12593791 Headache
125937911 12593791 Loss of libido
125937911 12593791 Male orgasmic disorder
125937911 12593791 Nightmare
125937911 12593791 Orgasmic sensation decreased
125937911 12593791 Sleep apnoea syndrome
125937911 12593791 Snoring
125937911 12593791 Throat tightness
125937911 12593791 Visual impairment

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125937911 12593791 1 201502 0