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
125645472 12564547 2 F 201510 20160907 20160718 20160913 EXP MX-ROCHE-1794156 ROCHE 46.99 YR F Y 72.00000 KG 20160913 CN MX MX

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
125645472 12564547 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 180 UG SOLUTION FOR INJECTION /wk
125645472 12564547 2 SS COPEGUS RIBAVIRIN 1 Oral 3 IN THE MORNING/2 AT NIGHT U 21511 200 MG TABLET
125645472 12564547 3 C ENALAPRIL ENALAPRIL 1 Oral 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125645472 12564547 1 Hepatitis C
125645472 12564547 2 Hepatitis C
125645472 12564547 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125645472 12564547 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125645472 12564547 Alopecia
125645472 12564547 Bone pain
125645472 12564547 Decreased appetite
125645472 12564547 Hepatitis
125645472 12564547 Somnolence
125645472 12564547 Weight decreased

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
125645472 12564547 1 20150804 0
125645472 12564547 2 20150804 0
125645472 12564547 3 2011 0