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
125662251 12566225 1 I 20160307 20160715 20160718 20160718 EXP FR-GUERBET LLC-1055191 GUERBET 88.00 YR F Y 0.00000 20160718 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
125662251 12566225 1 PS OPTIRAY IOVERSOL 1 Intravenous (not otherwise specified) 19710
125662251 12566225 2 SS CLAMOXYL (AMOXICILLIN HYDRATE) AMOXICILLIN 1 Intravenous (not otherwise specified) 0 4 G
125662251 12566225 3 SS MIRTAZAPINE. MIRTAZAPINE 1 Oral 0 15 MG
125662251 12566225 4 SS ACYCLOVIR. ACYCLOVIR 1 Intravenous (not otherwise specified) 0 500 MG
125662251 12566225 5 SS RAMIPRIL. RAMIPRIL 1 Intravenous (not otherwise specified) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125662251 12566225 1 Angiogram

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125662251 12566225 Acute kidney injury
125662251 12566225 Haematuria

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
125662251 12566225 1 20160301 20160301 0
125662251 12566225 2 20160226 20160307 0
125662251 12566225 3 20160226 20160307 0
125662251 12566225 4 20160226 20160303 0
125662251 12566225 5 20160302 20160302 0