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
125710142 12571014 2 F 201606 20160824 20160719 20160830 EXP US-GILEAD-2016-0221760 GILEAD 59.00 YR A M 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
125710142 12571014 1 PS LEDIPASVIR/SOFOSBUVIR LEDIPASVIRSOFOSBUVIR 1 Oral 1 DF, UNK 205834 1 DF TABLET
125710142 12571014 2 SS IMITREX SUMATRIPTAN SUCCINATE 1 Unknown UNK N 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125710142 12571014 1 Hepatitis C
125710142 12571014 2 Migraine

Outcome of event

Event ID CASEID OUTC COD
125710142 12571014 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125710142 12571014 Cerebral ischaemia
125710142 12571014 Confusional state
125710142 12571014 Dizziness
125710142 12571014 Drug interaction
125710142 12571014 Fatigue
125710142 12571014 Feeling cold
125710142 12571014 Flatulence
125710142 12571014 Nausea
125710142 12571014 Thirst

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
125710142 12571014 1 20160614 20160807 0
125710142 12571014 2 201604 0