The Safety Rates Drug Report

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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
125659422 12565942 2 F 20160812 20160718 20160822 EXP IT-TEVA-676424ACC TEVA SESSA M,ROSSI C,MASCOLO A,GRASSI E,FIORENTINO S,SCAVONE C. SUSPECTED ADVERSE REACTIONS TO CONTRAST MEDIA IN CAMPANIA REGION (ITALY): RESULTS FROM 14 YEARS OF POST-MARKETING SURVEILLANCE. EXPERT OPINION ON DRUG SAFETY. 2015 SEP 02;1341-1351. 49.00 YR F Y 0.00000 20160822 MD IT IT

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
125659422 12565942 1 PS FUROSEMIDE. FUROSEMIDE 1 U 18413
125659422 12565942 2 I Iomeprol IOMEPROL 1 Intravenous (not otherwise specified) 150 ML TOTAL U 0 150 ML
125659422 12565942 3 C LAMOTRIGINE. LAMOTRIGINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125659422 12565942 1 Product used for unknown indication
125659422 12565942 2 Product used for unknown indication
125659422 12565942 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125659422 12565942 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125659422 12565942 Blood pressure decreased
125659422 12565942 Drug interaction
125659422 12565942 Erythema
125659422 12565942 Heart rate increased
125659422 12565942 Rash erythematous

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found