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
79297854 7929785 4 F 201006 20160819 20110504 20160819 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-15709587 BRISTOL MYERS SQUIBB 38.34 YR F Y 0.00000 20160819 CN 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
79297854 7929785 1 PS REYATAZ ATAZANAVIR SULFATE 1 Oral 300 MG, QD U 21567 300 MG CAPSULE, HARD QD
79297854 7929785 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral UNK UNK, QD U 0 QD
79297854 7929785 3 SS NORVIR RITONAVIR 1 Oral 100 MG, QD U 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
79297854 7929785 1 Product used for unknown indication
79297854 7929785 2 Product used for unknown indication
79297854 7929785 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
79297854 7929785 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
79297854 7929785 Fallopian tube obstruction
79297854 7929785 Maternal exposure during pregnancy
79297854 7929785 Uterine dilation and curettage

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
79297854 7929785 1 20060313 0
79297854 7929785 2 20110316 0
79297854 7929785 3 20110316 0