The Safety Rates Drug Report

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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
124450022 12445002 2 F 201605 20160830 20160607 20160902 PER US-GLAXOSMITHKLINE-US2016GSK070748 GLAXOSMITHKLINE 65.51 YR F Y 81.65000 KG 20160902 OT 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
124450022 12445002 1 PS NARATRIPTAN NARATRIPTAN HYDROCHLORIDE 1 Oral 10 MG, SINGLE Y 20763 10 MG
124450022 12445002 2 SS IMITREX SUMATRIPTAN SUCCINATE 1 U 0
124450022 12445002 3 SS LEVAQUIN LEVOFLOXACIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124450022 12445002 1 Migraine
124450022 12445002 2 Product used for unknown indication
124450022 12445002 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124450022 12445002 Dizziness
124450022 12445002 Drug hypersensitivity
124450022 12445002 Drug ineffective
124450022 12445002 Erythema
124450022 12445002 Flushing
124450022 12445002 Hypotension
124450022 12445002 Limb injury
124450022 12445002 Malaise
124450022 12445002 Rash
124450022 12445002 Red cell distribution width increased
124450022 12445002 Syncope
124450022 12445002 Urticaria

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
124450022 12445002 1 20160507 20160507 0