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
127438311 12743831 1 I 20121026 20160502 20160914 20160914 EXP FR-GILEAD-2016-0211953 GILEAD 44.00 YR A M Y 0.00000 20160914 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
127438311 12743831 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral UNK Y 21752 TABLET
127438311 12743831 2 C INTELENCE ETRAVIRINE 1 Oral UNK 0
127438311 12743831 3 C ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral UNK 0
127438311 12743831 4 C NORVIR RITONAVIR 1 Oral UNK 0
127438311 12743831 5 C PREZISTA DARUNAVIR ETHANOLATE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127438311 12743831 1 HIV infection
127438311 12743831 2 HIV infection
127438311 12743831 3 HIV infection
127438311 12743831 4 HIV infection
127438311 12743831 5 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127438311 12743831 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127438311 12743831 Arthralgia
127438311 12743831 Bone pain
127438311 12743831 Hypophosphataemia

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
127438311 12743831 1 20090315 20160105 0
127438311 12743831 2 20090315 0
127438311 12743831 3 20090315 0
127438311 12743831 4 20090315 0
127438311 12743831 5 20090315 0