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
127030952 12703095 2 F 2007 20160921 20160831 20160926 PER US-GLAXOSMITHKLINE-US2016GSK123373 GLAXOSMITHKLINE 58.88 YR M Y 0.00000 20160926 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
127030952 12703095 1 PS IMITREX SUMATRIPTAN SUCCINATE 1 50 MG, UNK UNKNOWN 20132 50 MG TABLET
127030952 12703095 2 SS IMITREX SUMATRIPTAN SUCCINATE 1 100 MG, UNK UNKNOWN 20132 100 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127030952 12703095 1 Headache

Outcome of event

Event ID CASEID OUTC COD
127030952 12703095 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127030952 12703095 Bone pain
127030952 12703095 Cardiac disorder
127030952 12703095 Circumstance or information capable of leading to medication error
127030952 12703095 Ill-defined disorder
127030952 12703095 Myocardial infarction
127030952 12703095 Palpitations
127030952 12703095 Wrong technique in product usage process

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
127030952 12703095 1 2007 0