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
127883921 12788392 1 I 201609 20160923 20160928 20160928 PER US-PFIZER INC-2016449983 PFIZER 51.00 YR F Y 0.00000 20160928 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
127883921 12788392 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 75 MG, UNK U 20699 75 MG PROLONGED-RELEASE CAPSULE
127883921 12788392 2 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 UNK UNK, ALTERNATE DAY U 20699 PROLONGED-RELEASE CAPSULE QOD
127883921 12788392 3 SS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 UNK UNK, ALTERNATE DAY U 20699 QOD
127883921 12788392 4 SS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 U 20699

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127883921 12788392 1 Anxiety
127883921 12788392 2 Depression
127883921 12788392 3 Anxiety
127883921 12788392 4 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127883921 12788392 Dizziness
127883921 12788392 Emotional disorder
127883921 12788392 Intentional product use issue

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
127883921 12788392 2 201609 0
127883921 12788392 3 201609 0