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
127838241 12783824 1 I 201512 20160922 20160927 20160927 EXP FR-VIIV HEALTHCARE LIMITED-FR2016GSK140163 VIIV 51.55 YR M Y 0.00000 20160927 OT FR FR

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
127838241 12783824 1 PS TIVICAY DOLUTEGRAVIR SODIUM 1 Oral UNK 204790
127838241 12783824 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral UNK U 0
127838241 12783824 3 C ISENTRESS RALTEGRAVIR POTASSIUM 1 UNK D 0
127838241 12783824 4 C KIVEXA ABACAVIR SULFATELAMIVUDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127838241 12783824 1 HIV infection
127838241 12783824 2 HIV infection
127838241 12783824 3 HIV infection
127838241 12783824 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127838241 12783824 HO
127838241 12783824 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127838241 12783824 Arthralgia
127838241 12783824 Osteopenia

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
127838241 12783824 1 20151019 20160411 0
127838241 12783824 2 20151019 0