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
124815752 12481575 2 F 20160504 20160809 20160620 20160812 EXP IT-009507513-1606ITA008513 MERCK 80.00 YR F Y 0.00000 20160812 OT IT IT

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
124815752 12481575 1 SS ENALAPRIL MALEATE. ENALAPRIL MALEATE 1 Oral UNK, MONTHLY 0 10 MG TABLET /month
124815752 12481575 2 PS FUROSEMIDE. FUROSEMIDE 1 Oral 50 MG, DAILY 70017 50 MG TABLET QD
124815752 12481575 3 SS RISPERDAL RISPERIDONE 1 Oral 1 MG, DAILY 0 1 MG TABLET QD
124815752 12481575 4 C TAPAZOLE METHIMAZOLE 1 Oral U 0 TABLET
124815752 12481575 5 C PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 220 MG U 0 220 MG CAPSULE
124815752 12481575 6 C REPAGLINIDE. REPAGLINIDE 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124815752 12481575 1 Cardiac failure
124815752 12481575 2 Cardiac failure
124815752 12481575 3 Psychotic disorder
124815752 12481575 4 Hyperthyroidism
124815752 12481575 5 Atrial fibrillation
124815752 12481575 6 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124815752 12481575 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124815752 12481575 Hyponatraemia

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
124815752 12481575 1 201505 0
124815752 12481575 2 201505 0
124815752 12481575 3 200005 0
124815752 12481575 5 20151101 20160504 0
124815752 12481575 6 201405 0