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
75121644 7512164 4 F 20160827 20100730 20160827 EXP BR-BRISTOL-MYERS SQUIBB COMPANY-15212558 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160827 OT BR BR

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
75121644 7512164 1 PS DIDANOSINE. DIDANOSINE 1 Transplacental UNK U 20156
75121644 7512164 2 SS VIRACEPT NELFINAVIR MESYLATE 1 Transplacental UNK U 0
75121644 7512164 3 SS I RON FERROUS FUMARATE 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
75121644 7512164 1 Product used for unknown indication
75121644 7512164 2 Product used for unknown indication
75121644 7512164 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
75121644 7512164 OT
75121644 7512164 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
75121644 7512164 Anencephaly
75121644 7512164 Foetal 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
75121644 7512164 1 20030523 20030702 0
75121644 7512164 2 20030513 20030702 0