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
125039182 12503918 2 F 20160529 20160811 20160628 20160824 EXP IT-MINISAL02-363514 IT-TEVA-670734ACC TEVA 88.85 YR F Y 0.00000 20160825 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
125039182 12503918 1 PS ENALAPRIL ENALAPRIL 1 Oral 20 MILLIGRAM DAILY; U U 75479 20 MG
125039182 12503918 2 I MODURETIC 5-50 AMILORIDE HYDROCHLORIDEHYDROCHLOROTHIAZIDE 1 Oral 1 DOSAGE FORMS DAILY; U U 0 1 DF TABLET
125039182 12503918 3 C SINEMET CARBIDOPALEVODOPA 1 Oral 1.5 DOSAGE FORMS DAILY; U 0 1.5 DF TABLET
125039182 12503918 4 C PLASIL - 10 MG COMPRESSE 2 Oral U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125039182 12503918 1 Hypertension
125039182 12503918 2 Hypertension
125039182 12503918 3 Tremor
125039182 12503918 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125039182 12503918 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125039182 12503918 Drug interaction
125039182 12503918 Hyperkalaemia

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

no results found

Therapies reported

no results found