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
93705562 9370556 2 F 20130521 20130625 20130626 20130630 EXP FR-TEVA-415346ISR TEVA 72.51 YR M Y 0.00000 20130630 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
93705562 9370556 1 PS FUROSEMIDE TEVA 40 mg 1 ORAL 60 MILLIGRAM DAILY; 40 MG: MORNING, 20 MG :NOON. DIVISIBLE TABLETS D Y176 18413 TABLET BID
93705562 9370556 2 C JANUMET 1 ORAL 2 DOSAGE FORMS DAILY; D 0 1 DF BID
93705562 9370556 3 C PREVISCAN 20 mg 2 ORAL 15 MICROGRAM DAILY; SCORED TABLET, AT NIGHT D 0 TABLET QD
93705562 9370556 4 C ALDACTONE 1 ORAL D 0
93705562 9370556 5 C LERCAN 1 ORAL D 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
93705562 9370556 DE
93705562 9370556 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
93705562 9370556 Acute pulmonary oedema
93705562 9370556 Altered state of consciousness
93705562 9370556 Cardiac murmur
93705562 9370556 Cardio-respiratory arrest
93705562 9370556 Dermatitis
93705562 9370556 Hyperthermia
93705562 9370556 Leukocytosis
93705562 9370556 Myoclonus
93705562 9370556 Pneumonia aspiration
93705562 9370556 Rales
93705562 9370556 Somnolence

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
93705562 9370556 1 20130518 0
93705562 9370556 2 201305 0
93705562 9370556 3 201305 0
93705562 9370556 4 201305 0
93705562 9370556 5 201305 0