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
123487883 12348788 3 F 2016 20160715 20160509 20160725 PER US-PFIZER INC-2016217279 PFIZER 55.00 YR F Y 88.44000 KG 20160725 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
123487883 12348788 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, DAILY (AT BEDTIME) 21992 50 MG PROLONGED-RELEASE TABLET
123487883 12348788 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 21992 PROLONGED-RELEASE TABLET
123487883 12348788 3 C CELEBREX CELECOXIB 1 UNK 0
123487883 12348788 4 C LYRICA PREGABALIN 1 100 MG, UNK 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123487883 12348788 1 Depression
123487883 12348788 2 Fibromyalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123487883 12348788 Headache
123487883 12348788 Intentional product misuse
123487883 12348788 Migraine

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
123487883 12348788 1 2009 0
123487883 12348788 3 2009 0