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
127240001 12724000 1 I 20160313 0 20160907 20160907 DIR US-FDA-349780 FDA-CTU 37.00 YR F N 65.25000 KG 20160904 N 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
127240001 12724000 1 PS TOPAMAX TOPIRAMATE 1 Oral Y D 0
127240001 12724000 3 C HYDROCODONE HYDROCODONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127240001 12724000 1 Migraine

Outcome of event

Event ID CASEID OUTC COD
127240001 12724000 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127240001 12724000 Abdominal pain upper
127240001 12724000 Amnesia
127240001 12724000 Depression
127240001 12724000 Diarrhoea
127240001 12724000 Fatigue
127240001 12724000 Feeling abnormal
127240001 12724000 Impaired work ability
127240001 12724000 Menstrual disorder
127240001 12724000 Visual impairment
127240001 12724000 Vomiting
127240001 12724000 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
127240001 12724000 1 20160128 20160810 0