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
116310955 11631095 5 F 20160815 20151014 20160817 PER US-PFIZER INC-2015340731 PFIZER 61.00 YR M Y 0.00000 20160817 CN 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
116310955 11631095 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, UNK 20699 150 MG PROLONGED-RELEASE CAPSULE
116310955 11631095 2 I EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 225 MG, 1X/DAY AT NIGHT 20699 225 MG PROLONGED-RELEASE CAPSULE QD
116310955 11631095 3 I VIAGRA SILDENAFIL CITRATE 1 UNK 20895 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116310955 11631095 1 Depression
116310955 11631095 3 Erectile dysfunction

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
116310955 11631095 Drug interaction
116310955 11631095 Erectile dysfunction
116310955 11631095 Feeling abnormal
116310955 11631095 Grief reaction
116310955 11631095 Stress
116310955 11631095 Withdrawal syndrome

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

no results found

Therapies reported

no results found