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
126019941 12601994 1 I 20160602 20160721 20160728 20160728 EXP MD-GE HEALTHCARE MEDICAL DIAGNOSTICS-OMPQ-PR-1607S-1283 GE HEALTHCARE 35.00 YR F Y 75.00000 KG 20160728 MD MD MD

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
126019941 12601994 1 PS OMNIPAQUE IOHEXOL 1 Intravenous (not otherwise specified) 12629665 18956 90 ML SOLUTION FOR INJECTION
126019941 12601994 2 SS OMNIPAQUE IOHEXOL 1 12629665 18956
126019941 12601994 3 SS SODIUM CHLORIDE. SODIUM CHLORIDE 1 Intravenous (not otherwise specified) 0 5 ML SOLUTION FOR INJECTION
126019941 12601994 4 SS DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) 0 8 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126019941 12601994 1 Sarcoma uterus
126019941 12601994 2 Diagnostic procedure
126019941 12601994 3 Adjuvant therapy
126019941 12601994 4 Immune tolerance induction

Outcome of event

Event ID CASEID OUTC COD
126019941 12601994 LT
126019941 12601994 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126019941 12601994 Hyperhidrosis
126019941 12601994 Hypotension
126019941 12601994 Loss of consciousness
126019941 12601994 Muscle rigidity
126019941 12601994 Mydriasis
126019941 12601994 Pallor
126019941 12601994 Tremor

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
126019941 12601994 1 20160602 20160602 0
126019941 12601994 3 20160602 20160602 0
126019941 12601994 4 20160602 20160602 0