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
126135571 12613557 1 I 201502 20160719 20160802 20160802 EXP GB-MHRA-EYC 00142439 GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121136 RANBAXY 0.00 Y 0.00000 20160802 OT 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
126135571 12613557 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 91272 37.5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126135571 12613557 1 Depression

Outcome of event

Event ID CASEID OUTC COD
126135571 12613557 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126135571 12613557 Balance disorder
126135571 12613557 Breath sounds abnormal
126135571 12613557 Condition aggravated
126135571 12613557 Dry mouth
126135571 12613557 Dysgeusia
126135571 12613557 Headache
126135571 12613557 Loss of libido
126135571 12613557 Male orgasmic disorder
126135571 12613557 Nightmare
126135571 12613557 Orgasmic sensation decreased
126135571 12613557 Sleep apnoea syndrome
126135571 12613557 Snoring
126135571 12613557 Throat tightness
126135571 12613557 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
126135571 12613557 1 201502 0