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
118549872 11854987 2 F 20000331 20160826 20151221 20160826 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-11544392 BRISTOL MYERS SQUIBB 0.00 DY F Y 2.90000 KG 20160826 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
118549872 11854987 1 PS ZERIT STAVUDINE 1 Transplacental 40 MG, BID U 20412 40 MG CAPSULE, HARD BID
118549872 11854987 2 SS ZERIT STAVUDINE 1 Oral 1 MG/ML Y 0 3 MG ORAL SOLUTION BID
118549872 11854987 3 SS CRIXIVAN INDINAVIR SULFATE 1 Transplacental 400 MG, UNK U 0 400 MG
118549872 11854987 4 SS EPIVIR LAMIVUDINE 1 Transplacental 150 MG, BID U 0 150 MG BID
118549872 11854987 5 SS VIRAMUNE NEVIRAPINE 1 Oral 6 MG, ONE TIME DOSE Y 0 6 MG
118549872 11854987 6 SS VIRAMUNE NEVIRAPINE 1 Transplacental 200 MG, UNK U 0 200 MG
118549872 11854987 7 SS RETROVIR ZIDOVUDINE 1 Transplacental 200 MG, ONE TIME DOSE U 0 200 MG
118549872 11854987 8 SS SPASFON PHLOROGLUCINOL 1 Transplacental UNK U 0
118549872 11854987 9 SS SALBUTAMOL ALBUTEROL 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118549872 11854987 1 Product used for unknown indication
118549872 11854987 2 Prophylaxis
118549872 11854987 3 Product used for unknown indication
118549872 11854987 4 Product used for unknown indication
118549872 11854987 5 Prophylaxis
118549872 11854987 6 Product used for unknown indication
118549872 11854987 7 Product used for unknown indication
118549872 11854987 8 Product used for unknown indication
118549872 11854987 9 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118549872 11854987 OT
118549872 11854987 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118549872 11854987 Anaemia
118549872 11854987 Blood pyruvic acid decreased
118549872 11854987 Foetal exposure during pregnancy
118549872 11854987 Neutropenia
118549872 11854987 Skin depigmentation

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
118549872 11854987 1 20000331 0
118549872 11854987 2 20000331 20000512 0
118549872 11854987 3 20000331 0
118549872 11854987 4 20000331 0
118549872 11854987 5 20000402 20000402 0
118549872 11854987 6 20000331 20000331 0
118549872 11854987 7 20000331 20000331 0