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
117664373 11766437 3 F 20040523 20160908 20151123 20160914 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-15152028 BRISTOL MYERS SQUIBB 0.00 DY M Y 2.41000 KG 20160914 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
117664373 11766437 1 PS EFAVIRENZ EFAVIRENZ 1 Transplacental UNK 20972
117664373 11766437 2 SS LAMIVUDINE AND ZIDOVUDINE LAMIVUDINEIDOVUDINE 1 Transplacental UNK 0
117664373 11766437 3 SS LAMIVUDINE AND ZIDOVUDINE LAMIVUDINEIDOVUDINE 1 Transplacental UNK 0
117664373 11766437 4 SS LOPINAVIR + RITONAVIR LOPINAVIRRITONAVIR 1 Transplacental UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117664373 11766437 1 Product used for unknown indication
117664373 11766437 2 Product used for unknown indication
117664373 11766437 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117664373 11766437 OT
117664373 11766437 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
117664373 11766437 Congenital hydrocephalus
117664373 11766437 Foetal exposure during pregnancy
117664373 11766437 Neonatal gastrointestinal disorder
117664373 11766437 Premature baby

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
117664373 11766437 1 20000401 20040102 0
117664373 11766437 2 20010405 20040102 0
117664373 11766437 3 20040129 0
117664373 11766437 4 20040129 20040523 0