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
6809368 7326893 F 6809368-X 20100615 20100630 EXP GB-CUBIST-2010S1000113 CUBIST PHARMACEUTICALS, INC. 81 YR F Y 20100630 MD 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
6809368 1014003090 PS CUBICIN 1 INTRAVENOUS 021572
6809368 1014003091 SS CUBICIN 1 INTRAVENOUS 021572
6809368 1014003092 C VANCOMYCIN 1
6809368 1014003093 C GENTAMICIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6809368 1014003090 SOFT TISSUE INFECTION
6809368 1014003091 STAPHYLOCOCCAL BACTERAEMIA
6809368 1014003092 DRUG USE FOR UNKNOWN INDICATION
6809368 1014003093 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6809368 DE

Reactions reported

Event ID PT
6809368 ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT
6809368 RENAL FAILURE CHRONIC
6809368 STAPHYLOCOCCAL SEPSIS

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
6809368 1014003090 20100221
6809368 1014003091 20100221
6809368 1014003092 20100221