The Safety Rates Drug Report

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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
125283172 12528317 2 F 20151028 20160714 20160705 20160720 EXP IT-GILEAD-2016-0220741 GILEAD 46.00 YR A M Y 0.00000 20160720 PH IT IT

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
125283172 12528317 1 PS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral UNK Y 21752 TABLET
125283172 12528317 2 C TELZIR FOSAMPRENAVIR CALCIUM 1 Oral UNK 0
125283172 12528317 3 C NORVIR RITONAVIR 1 Oral 100 MG, UNK 0 100 MG
125283172 12528317 4 C DIBASE CHOLECALCIFEROL 1 Oral UNK 0
125283172 12528317 5 C LANSOPRAZOL MYLAN LANSOPRAZOLE 1 Oral UNK 0
125283172 12528317 6 C DELTACORTENE PREDNISONE 1 Oral 25 MG, UNK 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125283172 12528317 1 HIV infection
125283172 12528317 2 HIV infection
125283172 12528317 3 HIV infection
125283172 12528317 4 Vitamin D deficiency

Outcome of event

Event ID CASEID OUTC COD
125283172 12528317 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125283172 12528317 Diarrhoea
125283172 12528317 Dyslipidaemia
125283172 12528317 Hypophosphataemia
125283172 12528317 Osteoporosis

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
125283172 12528317 1 20150730 20151028 0
125283172 12528317 2 20140604 20160203 0
125283172 12528317 3 20140604 20160203 0
125283172 12528317 4 20140604 20160203 0
125283172 12528317 6 20150629 20151028 0