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
125788811 12578881 1 I 201607 20160709 20160721 20160721 PER US-PFIZER INC-2016339604 PFIZER 44.00 YR F Y 81.65000 KG 20160721 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
125788811 12578881 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, DAILY (EVERY DAY) U 21992 50 MG PROLONGED-RELEASE TABLET
125788811 12578881 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG EVERY TWO DAYS U 21992 50 MG PROLONGED-RELEASE TABLET QOD
125788811 12578881 3 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, EVERY THIRD DAY U 21992 50 MG PROLONGED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125788811 12578881 1 Anxiety

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125788811 12578881 Withdrawal syndrome

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
125788811 12578881 2 201607 0
125788811 12578881 3 201607 0