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
118975042 11897504 2 F 20000316 20160826 20160108 20160829 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-10913671 BRISTOL MYERS SQUIBB 0.00 DY M Y 2.97000 KG 20160829 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
118975042 11897504 1 PS VIDEX DIDANOSINE 1 Transplacental 150 MG, BID U 20156 150 MG TABLET BID
118975042 11897504 2 SS VIDEX DIDANOSINE 1 Oral UNK U 20156 POWDER FOR ORAL SOLUTION
118975042 11897504 3 SS CRIXIVAN INDINAVIR SULFATE 1 Transplacental UNK U 0
118975042 11897504 4 SS NORVIR RITONAVIR 1 Transplacental 300 MG, QD U 0 300 MG QD
118975042 11897504 5 SS VIRAMUNE NEVIRAPINE 1 Transplacental 200 MG, UNK U 0 200 MG
118975042 11897504 6 SS VIRAMUNE NEVIRAPINE 1 Oral 200 MG, UNK U 0 200 MG
118975042 11897504 7 SS ZIAGEN ABACAVIR SULFATE 1 Transplacental 300 MG, BID U 0 300 MG BID
118975042 11897504 8 C AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Transplacental UNK U 0
118975042 11897504 9 C I RON FERROUS FUMARATE 1 Transplacental UNK U 0
118975042 11897504 10 C GYNO PEVARYL ECONAZOLE NITRATE 1 Transplacental UNK U 0
118975042 11897504 11 C POLYGYNAX 2 Transplacental UNK U 0
118975042 11897504 12 C COLPOSEPTINE 2 Transplacental UNK U 0
118975042 11897504 13 C VITAMINS VITAMINS 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118975042 11897504 1 Product used for unknown indication
118975042 11897504 2 Product used for unknown indication
118975042 11897504 3 Product used for unknown indication
118975042 11897504 4 Product used for unknown indication
118975042 11897504 5 Product used for unknown indication
118975042 11897504 6 Product used for unknown indication
118975042 11897504 7 Product used for unknown indication
118975042 11897504 8 Product used for unknown indication
118975042 11897504 9 Product used for unknown indication
118975042 11897504 10 Product used for unknown indication
118975042 11897504 11 Product used for unknown indication
118975042 11897504 12 Product used for unknown indication
118975042 11897504 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118975042 11897504 OT
118975042 11897504 HO
118975042 11897504 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
118975042 11897504 Anaemia
118975042 11897504 Blood lactic acid increased
118975042 11897504 Foetal exposure during pregnancy
118975042 11897504 Hypertriglyceridaemia
118975042 11897504 Language disorder
118975042 11897504 Microcytosis
118975042 11897504 Neutropenia
118975042 11897504 Thalassaemia beta

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
118975042 11897504 1 20000316 0
118975042 11897504 2 20000316 20000427 0
118975042 11897504 3 20000316 0
118975042 11897504 4 20000316 0
118975042 11897504 5 20000316 20000316 0
118975042 11897504 6 20000317 20000317 0
118975042 11897504 7 20000316 0