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
125211791 12521179 1 I 20160622 20160701 20160701 EXP PHHY2016LT087188 SANDOZ BILIUKAS M, KARPAVICIENE V. CARDIAC AMYLOIDOSIS. MEDICINOS. 2015;21(4.3):873-80 57.00 YR M Y 0.00000 20160701 OT LT LT

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
125211791 12521179 1 PS METOPROLOL. METOPROLOL 1 Unknown 73288
125211791 12521179 2 SS TORASEMIDE TORSEMIDE 1 Unknown 0
125211791 12521179 3 SS CARVEDILOL. CARVEDILOL 1 Unknown 0
125211791 12521179 4 SS AMIODARONE AMIODARONE 1 Unknown 0
125211791 12521179 5 SS PERINDOPRIL PERINDOPRIL 1 Unknown 0
125211791 12521179 6 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 0
125211791 12521179 7 SS MILDRONATE MELDONIUM 1 Unknown 0
125211791 12521179 8 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 0
125211791 12521179 9 C WARFARIN WARFARIN 1 Unknown 0
125211791 12521179 10 C OXYGEN THERAPY OXYGEN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125211791 12521179 1 Product used for unknown indication
125211791 12521179 2 Product used for unknown indication
125211791 12521179 3 Product used for unknown indication
125211791 12521179 4 Product used for unknown indication
125211791 12521179 5 Product used for unknown indication
125211791 12521179 6 Product used for unknown indication
125211791 12521179 7 Product used for unknown indication
125211791 12521179 8 Product used for unknown indication
125211791 12521179 9 Product used for unknown indication
125211791 12521179 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125211791 12521179 DE
125211791 12521179 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125211791 12521179 Cardiac failure acute
125211791 12521179 Condition aggravated
125211791 12521179 Drug ineffective

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

no results found

Therapies reported

no results found