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
125437061 12543706 1 I 0 20160708 20160708 DIR 43.00 YR F N 120.00000 LBS 20160707 N 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
125437061 12543706 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 30 TABLET (S) IN THE MORNING TAKEN BY MOUTH N 0 30 DF COATED TABLET
125437061 12543706 3 C FISH OIL FISH OIL 1 0
125437061 12543706 5 C VITAMIN B12 CYANOCOBALAMIN 1 0
125437061 12543706 7 C IRON SUPPLEMENTS IRON 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125437061 12543706 1 Adjustment disorder with depressed mood

Outcome of event

Event ID CASEID OUTC COD
125437061 12543706 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125437061 12543706 Dizziness
125437061 12543706 Drug withdrawal syndrome
125437061 12543706 Fall
125437061 12543706 Gastrointestinal disorder
125437061 12543706 Impaired driving ability
125437061 12543706 Impaired work ability
125437061 12543706 Nausea
125437061 12543706 Paraesthesia
125437061 12543706 Suicidal ideation
125437061 12543706 Weight decreased

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
125437061 12543706 1 20130501 20160630 0