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
126523431 12652343 1 I 20160503 20160809 20160815 20160815 EXP IT-GILEAD-2016-0227909 GILEAD 50.00 YR A M Y 0.00000 20160815 PH IT IT

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
126523431 12652343 1 PS HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 1 DF, QD 167 DF 205834 1 DF TABLET QD
126523431 12652343 2 SS COPEGUS RIBAVIRIN 1 Oral 1.2 G, QD 200 G 0 1.2 G QD
126523431 12652343 3 C PAROXETIN /00830801/ PAROXETINE HYDROCHLORIDE 1 20 MG, UNK 0 20 MG
126523431 12652343 4 C SEROQUEL QUETIAPINE FUMARATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126523431 12652343 1 Hepatitis C
126523431 12652343 2 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
126523431 12652343 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126523431 12652343 Hepatocellular carcinoma

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
126523431 12652343 1 20151105 20160420 0
126523431 12652343 2 20151105 20160420 0