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
127988341 12798834 1 I 201609 20160926 20160930 20160930 EXP CL-VIIV HEALTHCARE LIMITED-CL2016GSK142115 VIIV 26.00 YR M Y 0.00000 20160930 MD CL CL

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
127988341 12798834 1 PS KIVEXA ABACAVIR SULFATELAMIVUDINE 1 UNK Y U 21652 FILM-COATED TABLET
127988341 12798834 2 SS REYATAZ ATAZANAVIR SULFATE 1 UNK Y U 0
127988341 12798834 3 C RITONAVIR. RITONAVIR 1 UNK 0
127988341 12798834 4 C ISENTRESS RALTEGRAVIR POTASSIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127988341 12798834 1 Antiretroviral therapy
127988341 12798834 2 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
127988341 12798834 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127988341 12798834 Diarrhoea
127988341 12798834 Gastrointestinal disorder
127988341 12798834 General physical health deterioration
127988341 12798834 Hyperbilirubinaemia
127988341 12798834 Jaundice
127988341 12798834 Nausea
127988341 12798834 Vomiting

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
127988341 12798834 1 20160913 201609 0
127988341 12798834 2 20160913 20160919 0
127988341 12798834 3 20160913 20160919 0
127988341 12798834 4 20160919 0