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
127206111 12720611 1 I 20160830 20160907 20160907 EXP FR-ASTELLAS-2016US033817 ASTELLAS 52.00 YR F Y 0.00000 20160907 CN US FR

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
127206111 12720611 1 PS TACROLIMUS. TACROLIMUS 1 Unknown 50 TO 10 NG/ML UNKNOWN FREQ. 50708 FORMULATION UNKNOWN
127206111 12720611 2 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK, UNKNOWN FREQ. (REDUCED BY 95%) U 50708 FORMULATION UNKNOWN
127206111 12720611 3 SS TELAPREVIR TELAPREVIR 1 Oral 0 750 MG TABLET TID
127206111 12720611 4 SS VIRAFERON INTERFERON ALFA-2B 1 Unknown 0 135 UG FORMULATION UNKNOWN /wk
127206111 12720611 5 SS VIRAFERON INTERFERON ALFA-2B 1 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
127206111 12720611 6 SS COPEGUS RIBAVIRIN 1 Unknown 0 714 MG FORMULATION UNKNOWN QD
127206111 12720611 7 SS COPEGUS RIBAVIRIN 1 Unknown UNK, UNKNOWN FREQ. 0 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127206111 12720611 1 Immunosuppression
127206111 12720611 3 Hepatitis C
127206111 12720611 4 Hepatitis C
127206111 12720611 6 Hepatitis C

Outcome of event

Event ID CASEID OUTC COD
127206111 12720611 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127206111 12720611 Anaemia
127206111 12720611 Drug interaction
127206111 12720611 Neutropenia
127206111 12720611 Thrombocytopenia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found