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
123204002 12320400 2 F 20160330 20160701 20160501 20160708 EXP FR-009507513-1604FRA014543 MERCK 72.15 YR M Y 0.00000 20160708 OT 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
123204002 12320400 1 PS IMIPENEM AND CILASTATIN CILASTATIN SODIUMIMIPENEM 1 Intravenous drip 2 G, 1 DAY 6 G Y 62756 2 G INTRAVENOUS INJECTION QD
123204002 12320400 2 SS ZYLORIC ALLOPURINOL 1 Oral 100 MG, 1 DAY 1400 MG Y 0 100 MG TABLET QD
123204002 12320400 3 SS INEXIUM (esomeprazole magnesium) ESOMEPRAZOLE MAGNESIUM 1 Oral UNK Y 0
123204002 12320400 4 SS CIFLOX (ciprofloxacin hydrochloride) CIPROFLOXACIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) 800 MG, UNK Y 0 800 MG SOLUTION FOR INJECTION/INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123204002 12320400 1 Pseudomonas infection
123204002 12320400 2 Gout
123204002 12320400 3 Gastrooesophageal reflux disease
123204002 12320400 4 Pseudomonas infection

Outcome of event

Event ID CASEID OUTC COD
123204002 12320400 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123204002 12320400 Acute generalised exanthematous pustulosis

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
123204002 12320400 1 20160328 20160330 0
123204002 12320400 2 20160317 20160331 0
123204002 12320400 3 20160215 20160401 0
123204002 12320400 4 20160328 20160401 0