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
126556861 12655686 1 I 20150902 20160816 20160816 PER US-ROCHE-1629845 ROCHE 0.00 F Y 0.00000 20160816 CN US US

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
126556861 12655686 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous U 103964 180 MG /wk
126556861 12655686 2 SS PEGASYS PEGINTERFERON ALFA-2A 1 U 103964
126556861 12655686 3 C ENTECAVIR. ENTECAVIR 1 Oral 0 .5 MG QD
126556861 12655686 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 0 500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126556861 12655686 1 Hepatitis B
126556861 12655686 2 Hepatitis D
126556861 12655686 3 Hepatitis B
126556861 12655686 4 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126556861 12655686 Asthenia
126556861 12655686 Feeling cold
126556861 12655686 Headache
126556861 12655686 Musculoskeletal discomfort
126556861 12655686 Pain
126556861 12655686 Pyrexia

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

no results found

Therapies reported

no results found