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
125501892 12550189 2 F 20160720 20160712 20160727 EXP US-GILEAD-2016-0222250 GILEAD 66.00 YR E M Y 0.00000 20160727 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
125501892 12550189 1 PS LEDIPASVIR/SOFOSBUVIR LEDIPASVIRSOFOSBUVIR 1 Oral 1 UNK, UNK Y 205834 1 DF TABLET QD
125501892 12550189 2 SS RIBAVIRIN. RIBAVIRIN 1 Unknown UNK Y 0
125501892 12550189 3 C CENTRUM SILVER /02363801/ MINERALSVITAMINS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125501892 12550189 1 Hepatitis C
125501892 12550189 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125501892 12550189 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125501892 12550189 Blood count abnormal
125501892 12550189 Chromaturia
125501892 12550189 Haematocrit decreased
125501892 12550189 Haemoglobin decreased
125501892 12550189 Hepatic cirrhosis
125501892 12550189 Insomnia
125501892 12550189 Pollakiuria
125501892 12550189 Seasonal allergy

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
125501892 12550189 1 20160614 0
125501892 12550189 2 201606 0