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
93730182 9373018 2 F 2013 20130624 20130627 20130630 EXP FR-TEVA-415706ISR TEVA 89.00 YR F Y 0.00000 20130630 CN 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
93730182 9373018 1 PS FUROSEMIDE TEVA 1 250 MILLIGRAM DAILY; D 18413 .5 DF TABLET QD
93730182 9373018 2 SS FUROSEMIDE TEVA 1 375 MILLIGRAM DAILY; D 18413 .75 DF TABLET QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
93730182 9373018 DE
93730182 9373018 OT
93730182 9373018 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
93730182 9373018 Aphagia
93730182 9373018 Death
93730182 9373018 Drug ineffective
93730182 9373018 Fatigue
93730182 9373018 Gait disturbance
93730182 9373018 Induration
93730182 9373018 Oedema peripheral
93730182 9373018 Secretion discharge
93730182 9373018 Somnolence
93730182 9373018 Weight increased

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
93730182 9373018 2 201304 0