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
121341613 12134161 3 F 20160224 20160705 20160301 20160718 EXP US-GLAXOSMITHKLINE-US2016027145 GLAXOSMITHKLINE 67.36 YR F Y 74.00000 KG 20160718 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
121341613 12134161 1 PS IMITREX SUMATRIPTAN SUCCINATE 1 Subcutaneous 6 MG, U U SV150809 20080 6 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
121341613 12134161 2 SS IMITREX SUMATRIPTAN SUCCINATE 1 UNK U SV141919 20080 SOLUTION FOR INJECTION IN PRE-FILLED PEN
121341613 12134161 3 SS IMITREX SUMATRIPTAN SUCCINATE 1 UNK U C717939 20080 SOLUTION FOR INJECTION IN PRE-FILLED PEN
121341613 12134161 4 SS IMITREX SUMATRIPTAN SUCCINATE 1 UNK, U U C716202 20080 SOLUTION FOR INJECTION IN PRE-FILLED PEN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121341613 12134161 1 Migraine with aura

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121341613 12134161 Injection site reaction
121341613 12134161 Product quality issue
121341613 12134161 Syringe issue

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found