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
125447831 12544783 1 I 201601 20160413 20160711 20160711 EXP CN-VIIV HEALTHCARE LIMITED-CN2016GSK093457 VIIV 47.00 YR M Y 0.00000 20160711 CN CN CN

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
125447831 12544783 1 PS LAMIVUDINE. LAMIVUDINE 1 UNK N U 21003
125447831 12544783 2 SS ADEFOVIR DIPIVOXIL. ADEFOVIR DIPIVOXIL 1 UNK N U 0
125447831 12544783 3 SS VIREAD TENOFOVIR DISOPROXIL FUMARATE 1 Oral UNK, 300 MG 0 TABLET
125447831 12544783 4 SS Telbivudine TELBIVUDINE 1 UNK N 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125447831 12544783 1 Hepatitis B
125447831 12544783 2 Hepatitis B
125447831 12544783 3 Hepatitis B
125447831 12544783 4 Hepatitis B

Outcome of event

Event ID CASEID OUTC COD
125447831 12544783 OT
125447831 12544783 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125447831 12544783 Blood creatine phosphokinase increased
125447831 12544783 Drug tolerance
125447831 12544783 Hepatic cirrhosis
125447831 12544783 Product use issue

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

no results found

Therapies reported

no results found