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
5232798 6239329 I 5232798-7 20070126 20070206 DIR 58 YR M N 120 LBS 20070201 PH N N UNITED STATES

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
5232798 1008126896 PS CIPRO 1 ORAL 750 MG Q12HRS PO Y D
5232798 1008154842 SS ERTAPENEM 1 GM 2 INTRAVENOUS 1 GM DAILY IV Y D

Indications of drugs used

Event ID DRUG SEQ INDI PT
5232798 1008126896 ABSCESS
5232798 1008126896 PNEUMONIA
5232798 1008154842 ABSCESS
5232798 1008154842 PNEUMONIA

Outcome of event

Event ID OUTC COD
5232798 HO

Reactions reported

Event ID PT
5232798 DIARRHOEA
5232798 EOSINOPHILIA
5232798 GLOMERULONEPHRITIS
5232798 LEUKOCYTURIA
5232798 NEPHRITIS INTERSTITIAL
5232798 RENAL FAILURE ACUTE
5232798 UNEVALUABLE EVENT

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
5232798 1008126896 20070112 20070126
5232798 1008154842 20070112 20070126