The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
5201024 6359460 I 5201024-7 20051216 20070103 20070108 EXP GB-GLAXOSMITHKLINE-B0453093A GLAXOSMITHKLINE 12 YR F Y 20070108 CN UNITED KINGDOM

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
5201024 1008019300 PS AUGMENTIN '125' 1 INTRAVENOUS 50564
5201024 1008019301 SS CEFOTAXIME SODIUM 1 INTRAVENOUS
5201024 1008019302 SS FLAGYL 1 INTRAVENOUS
5201024 1008019303 SS FLUCLOXACILLIN 2 INTRAVENOUS
5201024 1008019304 SS MEROPENEM 2 INTRAVENOUS
5201024 1008019305 C FLUTICASONE PROPIONATE 1 NASAL
5201024 1008019306 C ACETAMINOPHEN 1
5201024 1008019307 C PIRITON 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5201024 1008019300 DRUG USE FOR UNKNOWN INDICATION
5201024 1008019301 EMPYEMA
5201024 1008019304 EMPYEMA
5201024 1008019305 SINUSITIS

Outcome of event

Event ID OUTC COD
5201024 OT

Reactions reported

Event ID PT
5201024 ALANINE AMINOTRANSFERASE INCREASED
5201024 ERYTHEMA
5201024 NEUTROPENIA
5201024 OEDEMA
5201024 PYREXIA
5201024 RASH
5201024 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
5201024 1008019300 20051201 20051203 3 DAY
5201024 1008019301 20051203 20051218 16 DAY
5201024 1008019302 20051203 20051218 16 DAY
5201024 1008019303 20051203 20051218 16 DAY
5201024 1008019304 20051218 20051222 5 DAY
5201024 1008019305 20051203
5201024 1008019306 20051201