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
127349551 12734955 1 I 20140627 20160829 20160912 20160912 EXP ES-AGEMED-341564440 ES-VALIDUS PHARMACEUTICALS LLC-ES-2016VAL002590 VALIDUS 82.00 YR M Y 0.00000 20160912 MD ES ES

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
127349551 12734955 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral 40 MG, QD Y 16273 40 MG
127349551 12734955 2 SS POTASION POTASSIUM CHLORIDE 1 Oral 390 MG, QD Y 0 390 MG CAPSULE, HARD
127349551 12734955 3 C WARFARIN WARFARIN 1 UNK Y 0
127349551 12734955 4 C GABAPENTIN. GABAPENTIN 1 UNK Y 0
127349551 12734955 5 C IBUPROFENO IBUPROFEN 1 UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127349551 12734955 1 Cardiac failure
127349551 12734955 2 Hypokalaemia
127349551 12734955 3 Product used for unknown indication
127349551 12734955 4 Product used for unknown indication
127349551 12734955 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127349551 12734955 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127349551 12734955 Acute kidney injury
127349551 12734955 Atrial fibrillation
127349551 12734955 Hyperkalaemia

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
127349551 12734955 1 20140701 0
127349551 12734955 2 201310 20140701 0
127349551 12734955 3 20140601 0
127349551 12734955 4 20140701 0
127349551 12734955 5 20140624 20140701 0