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
127630931 12763093 1 I 20160219 20160714 20160920 20160920 EXP PT-INFARMED-S201605-96 PT-009507513-1607PRT006491 MERCK 71.28 YR F Y 0.00000 20160920 CN PT PT

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
127630931 12763093 1 PS REBETOL RIBAVIRIN 1 Oral 200 MG, 5 TIMES PER DAY, Y 20903 200 MG CAPSULE
127630931 12763093 2 SS COPEGUS RIBAVIRIN 1 Oral 3 COMPRIMIDOS AO ALMO?O + 2 COMPRIMIDOS AO JANTAR 0 200 MG FILM-COATED TABLET
127630931 12763093 3 SS HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 1 DF (90 MG + 400 MG), QD 0 1 DF FILM-COATED TABLET QD
127630931 12763093 4 C CONCOR BISOPROLOL FUMARATE 1 Oral 10 MG, UNK U 0 10 MG COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127630931 12763093 1 Chronic hepatitis C
127630931 12763093 2 Chronic hepatitis C
127630931 12763093 3 Chronic hepatitis C
127630931 12763093 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127630931 12763093 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127630931 12763093 Diarrhoea
127630931 12763093 Flatulence
127630931 12763093 Insomnia
127630931 12763093 Localised oedema
127630931 12763093 Melaena
127630931 12763093 Oedema peripheral
127630931 12763093 Rectal discharge

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
127630931 12763093 1 20160212 20160311 0
127630931 12763093 2 20160312 0
127630931 12763093 3 20160212 0