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
125926572 12592657 2 F 20160509 20160722 20160726 20160805 EXP AN20160721 FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002317 VALIDUS 83.00 YR F Y 0.00000 20160805 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
125926572 12592657 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral 1 DF, DAILY Y UNK 16273 1 DF TABLET
125926572 12592657 2 I TELMISARTAN. TELMISARTAN 1 Oral 80 MG, DAILY Y UNK 0 80 MG TABLET
125926572 12592657 3 I SELOKEN /00376902/ METOPROLOL TARTRATE 1 Oral 1 DF, TWICE A DAY UNK 0 1 DF
125926572 12592657 4 I DIFFU K POTASSIUM CHLORIDE 1 Oral 2 DF, DAILY Y UNK 0 2 DF CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125926572 12592657 1 Hypertension
125926572 12592657 2 Hypertension
125926572 12592657 3 Product used for unknown indication
125926572 12592657 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125926572 12592657 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125926572 12592657 Electrocardiogram abnormal
125926572 12592657 Hyperkalaemia
125926572 12592657 Renal failure

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
125926572 12592657 1 201605 0
125926572 12592657 2 20160511 0
125926572 12592657 4 20160509 0