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
127978621 12797862 1 I 201609 20160926 20160930 20160930 EXP CL-GLAXOSMITHKLINE-CL2016GSK142115 GLAXOSMITHKLINE 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
127978621 12797862 1 PS KIVEXA ABACAVIR SULFATELAMIVUDINE 1 UNK Y U 21652 FILM-COATED TABLET
127978621 12797862 2 SS REYATAZ ATAZANAVIR SULFATE 1 UNK Y U 0
127978621 12797862 3 C RITONAVIR. RITONAVIR 1 UNK 0
127978621 12797862 4 C ISENTRESS RALTEGRAVIR POTASSIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127978621 12797862 1 Antiretroviral therapy
127978621 12797862 2 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
127978621 12797862 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127978621 12797862 Diarrhoea
127978621 12797862 Gastrointestinal disorder
127978621 12797862 General physical health deterioration
127978621 12797862 Hyperbilirubinaemia
127978621 12797862 Jaundice
127978621 12797862 Nausea
127978621 12797862 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
127978621 12797862 1 20160913 201609 0
127978621 12797862 2 20160913 20160919 0
127978621 12797862 3 20160913 20160919 0
127978621 12797862 4 20160919 0