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
120699343 12069934 3 F 201512 20160912 20160211 20160921 EXP GB-MHRA-EYC 00134185 GB-CIPLA LTD.-2016GB01101 CIPLA 0.00 Y 0.00000 20160921 OT GB GB

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
120699343 12069934 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral 50 MG, BID Y U 76343 50 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120699343 12069934 1 Migraine

Outcome of event

Event ID CASEID OUTC COD
120699343 12069934 HO
120699343 12069934 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120699343 12069934 Central nervous system lesion
120699343 12069934 Headache
120699343 12069934 Noninfective encephalitis
120699343 12069934 Vomiting

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
120699343 12069934 1 201509 201512 0