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
125322421 12532242 1 I 20160417 20160627 20160706 20160706 EXP US-GILEAD-2016-0221354 GILEAD 36.00 YR A F Y 0.00000 20160706 OT US US

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
125322421 12532242 1 PS EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EMTRICITABINETENOFOVIR DISOPROXIL 1 Oral 1 DF, QD 21752 1 DF TABLET QD
125322421 12532242 2 SS TIVICAY DOLUTEGRAVIR SODIUM 1 Oral 1 DF, QD U 0 1 DF QD
125322421 12532242 3 SS REYATAZ ATAZANAVIR SULFATE 1 Oral 300 MG, QD 0 300 MG QD
125322421 12532242 4 SS NORVIR RITONAVIR 1 Oral 1 DF, QD 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125322421 12532242 1 HIV infection
125322421 12532242 2 HIV infection
125322421 12532242 3 HIV infection
125322421 12532242 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125322421 12532242 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125322421 12532242 Abortion spontaneous
125322421 12532242 Maternal exposure during pregnancy

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
125322421 12532242 2 20160525 0
125322421 12532242 3 20160525 0
125322421 12532242 4 20160525 0