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
126387391 12638739 1 I 20160620 20160801 20160809 20160809 EXP GB-MHRA-EYC 00142954 PHHY2016GB105642 SANDOZ 32.00 YR M Y 90.00000 KG 20160809 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
126387391 12638739 1 PS TOPIRAMATE. TOPIRAMATE 1 Oral 100 MG, QD 4973.95801 MG 79206 100 MG QD
126387391 12638739 2 SS TOPIRAMATE. TOPIRAMATE 1 Oral 25 MG, QD 4973.95801 MG 79206 25 MG QD
126387391 12638739 3 SS TOPIRAMATE. TOPIRAMATE 1 Oral 75 MG, QD 4973.95801 MG 79206 75 MG QD
126387391 12638739 4 C CITALOPRAM HYDROBROMIDE. CITALOPRAM HYDROBROMIDE 1 Unknown U 0
126387391 12638739 5 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown U 0
126387391 12638739 6 C SUMATRIPTAN SUCCINATE. SUMATRIPTAN SUCCINATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126387391 12638739 1 Migraine prophylaxis
126387391 12638739 4 Product used for unknown indication
126387391 12638739 5 Product used for unknown indication
126387391 12638739 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126387391 12638739 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126387391 12638739 Pain in extremity
126387391 12638739 Paraesthesia

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
126387391 12638739 2 20151204 0