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
126966781 12696678 1 I 20160829 20160830 20160830 EXP GB-MHRA-EYC 00144285 GB-ROCHE-1822048 ROCHE 18.00 YR F Y 31.25000 KG 20160830 MD GB GB

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
126966781 12696678 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous N U 103964 180 UG SOLUTION FOR INJECTION
126966781 12696678 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous N U 103964 135 UG SOLUTION FOR INJECTION
126966781 12696678 3 C CARBIMAZOLE CARBIMAZOLE 1 Unknown 0
126966781 12696678 4 C FORCEVAL FOLIC ACIDIRONMINERALSVITAMINS 1 Unknown 0
126966781 12696678 5 C PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126966781 12696678 1 Chronic hepatitis B
126966781 12696678 2 Chronic hepatitis B

Outcome of event

Event ID CASEID OUTC COD
126966781 12696678 HO
126966781 12696678 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126966781 12696678 Abnormal loss of weight
126966781 12696678 Asthenia
126966781 12696678 Demyelinating polyneuropathy
126966781 12696678 Muscle atrophy

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
126966781 12696678 1 20151106 20160407 0
126966781 12696678 2 20160408 20160729 0