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
125419132 12541913 2 F 20160622 20160727 20160708 20160803 EXP IT-MINISAL02-365281 IT-MYLANLABS-2016M1027851 MYLAN 0.00 Y 0.00000 20160803 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
125419132 12541913 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral 100 MG, QD U U 18487 100 MG TABLET QD
125419132 12541913 2 SS POTASSIUM CANRENOATE CANRENOATE POTASSIUM 1 Oral 50 MG, QD U U 0 50 MG QD
125419132 12541913 3 C TRITTICO TRAZODONE HYDROCHLORIDE 1 Oral 15 DF 0 15 DF ORAL DROPS, SOLUTION
125419132 12541913 4 C COUMADIN WARFARIN SODIUM 1 0 TABLET
125419132 12541913 5 C CARVEDILOL. CARVEDILOL 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125419132 12541913 1 Product used for unknown indication
125419132 12541913 2 Product used for unknown indication
125419132 12541913 3 Product used for unknown indication
125419132 12541913 4 Product used for unknown indication
125419132 12541913 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125419132 12541913 HO
125419132 12541913 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125419132 12541913 Dehydration
125419132 12541913 Disorientation
125419132 12541913 Hypokalaemia
125419132 12541913 Hyponatraemia
125419132 12541913 Loss of consciousness
125419132 12541913 Sopor

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
125419132 12541913 1 20160101 0
125419132 12541913 2 20160101 0