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
112385682 11238568 2 F 20160718 20150706 20160726 EXP CA-GILEAD-2014-0116980 GILEAD 61.00 YR A F Y 0.00000 20160726 OT CA CA

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
112385682 11238568 1 PS SOVALDI SOFOSBUVIR 1 Oral 400 MG, QD U 204671 400 MG TABLET QD
112385682 11238568 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous 180 ?G, UNK U 0 180 UG /wk
112385682 11238568 3 SS COPEGUS RIBAVIRIN 1 Oral 1200 MG, QD U 0 1200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112385682 11238568 1 Chronic hepatitis C
112385682 11238568 2 Chronic hepatitis C
112385682 11238568 3 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
112385682 11238568 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112385682 11238568 Cheilitis
112385682 11238568 Dry skin
112385682 11238568 Hepatic enzyme increased
112385682 11238568 Lip dry
112385682 11238568 Pain
112385682 11238568 Skin irritation

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
112385682 11238568 1 20140702 20140924 0
112385682 11238568 2 20140702 20140924 0
112385682 11238568 3 20140702 20140924 0