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
126802292 12680229 2 F 20160813 20160815 20160824 20160830 PER US-GLAXOSMITHKLINE-US2016118129 GLAXOSMITHKLINE 62.13 YR F Y 0.00000 20160830 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
126802292 12680229 1 PS IMITREX SUMATRIPTAN SUCCINATE 1 Nasal 20 MG, PRN U J047 20626 20 MG NASAL SPRAY
126802292 12680229 2 SS IMITREX SUMATRIPTAN SUCCINATE 1 UNK, U U 0 SOLUTION FOR INJECTION IN PRE-FILLED PEN
126802292 12680229 3 C ARMOUR THYROID THYROID, PORCINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126802292 12680229 1 Migraine
126802292 12680229 2 Migraine

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126802292 12680229 Drug ineffective
126802292 12680229 Inappropriate schedule of drug administration
126802292 12680229 Overdose
126802292 12680229 Product quality issue
126802292 12680229 Product supply issue

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
126802292 12680229 1 2015 0