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
123893572 12389357 2 F 2015 20160701 20160520 20160706 EXP BR-PFIZER INC-2016233683 PFIZER 47.00 YR F Y 0.00000 20160706 CN BR BR

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
123893572 12389357 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 100 MG, 1X/DAY U 99758 21992 100 MG PROLONGED-RELEASE TABLET QD
123893572 12389357 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 75 MG, 1X/DAY U 21992 75 MG PROLONGED-RELEASE TABLET QD
123893572 12389357 3 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY U 21992 50 MG PROLONGED-RELEASE TABLET QD
123893572 12389357 4 C EUTHYROX LEVOTHYROXINE SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123893572 12389357 1 Depression
123893572 12389357 2 Panic disorder
123893572 12389357 4 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
123893572 12389357 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123893572 12389357 Amnesia
123893572 12389357 Drug dependence
123893572 12389357 Dyspnoea
123893572 12389357 Fear
123893572 12389357 Malaise
123893572 12389357 Panic disorder
123893572 12389357 Sinusitis
123893572 12389357 Tachycardia

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
123893572 12389357 1 2009 0
123893572 12389357 2 2013 0
123893572 12389357 3 2013 0
123893572 12389357 4 1996 0