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
125510851 12551085 1 I 20160531 20160707 20160713 20160713 EXP CH-ROCHE-1791741 ROCHE 58.00 YR M Y 74.00000 KG 20160713 MD CH CH

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
125510851 12551085 1 PS COPEGUS RIBAVIRIN 1 Unknown 21511
125510851 12551085 2 SS SOVALDI SOFOSBUVIR 1 Oral 0 400 MG
125510851 12551085 3 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown 0
125510851 12551085 4 C TRIATEC (CODEINE PHOSPHATE/PARACETAMOL) 2 0
125510851 12551085 5 C SPIRICORT PREDNISOLONE 1 0
125510851 12551085 6 C PANTOZOL (SWITZERLAND) PANTOPRAZOLE SODIUM 1 0
125510851 12551085 7 C IMUREK AZATHIOPRINE 1 0
125510851 12551085 8 C CALCIMAGON-D3 CALCIUMCHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125510851 12551085 1 Chronic hepatitis C
125510851 12551085 2 Chronic hepatitis C

Outcome of event

Event ID CASEID OUTC COD
125510851 12551085 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125510851 12551085 Drug ineffective
125510851 12551085 Hepatitis C
125510851 12551085 Incorrect drug administration duration

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
125510851 12551085 1 20151125 20160216 0
125510851 12551085 2 20151125 20160216 0