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
126047681 12604768 1 I 20160601 20160715 20160728 20160728 EXP CN20160465 FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002336 VALIDUS 84.00 YR F Y 0.00000 20160728 OT FR FR

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
126047681 12604768 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral 40 MG, DAILY 16273 40 MG
126047681 12604768 2 SS FOZITEC /00915301/ FOSINOPRIL 1 Oral 10 MG, DAILY Y 0 10 MG
126047681 12604768 3 SS CARDENSIEL BISOPROLOL FUMARATE 1 Oral 10 MG, DAILY 0 10 MG
126047681 12604768 4 SS DIFFU K POTASSIUM CHLORIDE 1 Oral 600 MG, DAILY Y 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126047681 12604768 1 Cardiac failure
126047681 12604768 2 Cardiac failure
126047681 12604768 3 Cardiac failure
126047681 12604768 4 Cardiac failure

Outcome of event

Event ID CASEID OUTC COD
126047681 12604768 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126047681 12604768 Acute kidney injury
126047681 12604768 Confusional state
126047681 12604768 Hallucination

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
126047681 12604768 1 20160527 0
126047681 12604768 2 20160527 20160601 0
126047681 12604768 3 20160527 0
126047681 12604768 4 20160527 20160601 0