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
125305941 12530594 1 I 20160412 20160706 20160706 EXP US-GLAXOSMITHKLINE-US2016049697 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160706 CN 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
125305941 12530594 1 PS IMITREX SUMATRIPTAN SUCCINATE 1 100 MG, UNK 20132 100 MG TABLET
125305941 12530594 2 SS IMITREX SUMATRIPTAN SUCCINATE 1 UNK 0 NASAL SPRAY
125305941 12530594 3 C AMBIEN ZOLPIDEM TARTRATE 1 U 0
125305941 12530594 4 C ATIVAN LORAZEPAM 1 U 0
125305941 12530594 5 C CYCLOBENZAPRINE CYCLOBENZAPRINE 1 U 0
125305941 12530594 6 C LYRICA PREGABALIN 1 U 0
125305941 12530594 7 C TOPAMAX TOPIRAMATE 1 U 0
125305941 12530594 8 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125305941 12530594 1 Migraine
125305941 12530594 2 Migraine

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125305941 12530594 Drug ineffective

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
125305941 12530594 2 201603 0