The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5200902 6359459 I 5200902-2 20051216 20061229 20070108 EXP GB-AVENTIS-200710008GDDC AVENTIS PHARMACEUTICALS, INC. 12 YR F Y 20070108

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5200902 1008018798 PS FLAGYL 1 INTRAVENOUS UNK 20743
5200902 1008018799 SS CEFOTAXIME SODIUM 1 INTRAVENOUS UNK 050547
5200902 1008018800 SS FLUCLOXACILLIN 2 INTRAVENOUS UNK
5200902 1008018801 SS AUGMENTIN '125' 1 INTRAVENOUS DOSE: 1.2 G UNK
5200902 1008018802 SS MEROPENEM 2 INTRAVENOUS DOSE: 1.7G UNK
5200902 1008018803 C FLUTICASONE PROPIONATE 1 NASAL UNK
5200902 1008018804 C ACETAMINOPHEN 1 UNK
5200902 1008018805 C PIRITON 2 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
5200902 1008018799 EMPYEMA
5200902 1008018802 EMPYEMA
5200902 1008018803 SINUSITIS
5200902 1008018804 PYREXIA

Outcome of event

Event ID OUTC COD
5200902 OT

Reactions reported

Event ID PT
5200902 ALANINE AMINOTRANSFERASE INCREASED
5200902 ERYTHEMA
5200902 NEUTROPENIA
5200902 OEDEMA
5200902 RASH
5200902 THROMBOCYTOPENIA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5200902 1008018798 20051203 20051218
5200902 1008018799 20051203 20051218
5200902 1008018800 20051203 20051218
5200902 1008018801 20051201 20051203
5200902 1008018802 20051218 20051222
5200902 1008018803 20051203
5200902 1008018804 20051201