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
126063351 12606335 1 I 201502 20160719 20160729 20160729 EXP GB-MHRA-EYC 00142439 GB-TEVA-679613ACC TEVA 57.00 YR M Y 80.73000 KG 20160729 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
126063351 12606335 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MILLIGRAM DAILY; U 76690 37.5 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126063351 12606335 1 Depression

Outcome of event

Event ID CASEID OUTC COD
126063351 12606335 OT
126063351 12606335 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126063351 12606335 Balance disorder
126063351 12606335 Breath sounds abnormal
126063351 12606335 Condition aggravated
126063351 12606335 Dry mouth
126063351 12606335 Dysgeusia
126063351 12606335 Headache
126063351 12606335 Loss of libido
126063351 12606335 Male orgasmic disorder
126063351 12606335 Nightmare
126063351 12606335 Orgasmic sensation decreased
126063351 12606335 Sleep apnoea syndrome
126063351 12606335 Snoring
126063351 12606335 Throat tightness
126063351 12606335 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
126063351 12606335 1 201502 0