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
87094205 8709420 5 F 2012 20160822 20120806 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-16806127 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160824 CN US 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
87094205 8709420 1 PS REYATAZ ATAZANAVIR SULFATE 1 Transplacental UNK U 21567
87094205 8709420 2 C NORVIR RITONAVIR 1 Transplacental UNK U 0
87094205 8709420 3 C TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87094205 8709420 1 Product used for unknown indication
87094205 8709420 2 Product used for unknown indication
87094205 8709420 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
87094205 8709420 OT
87094205 8709420 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
87094205 8709420 Anal atresia
87094205 8709420 Bladder dilatation
87094205 8709420 Dysmorphism
87094205 8709420 Eagle Barrett syndrome
87094205 8709420 Foetal exposure during pregnancy
87094205 8709420 Intestinal malrotation
87094205 8709420 Persistent cloaca
87094205 8709420 Renal aplasia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found