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
126690371 12669037 1 I 20140820 20160819 20160819 EXP NL-LRB-180253 NL-009507513-1408NLD012014 MERCK 0.00 M Y 0.00000 20160819 OT NL NL

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
126690371 12669037 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 1DD1 Y 19766 40 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126690371 12669037 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126690371 12669037 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126690371 12669037 Inguinal hernia
126690371 12669037 Muscle contractions involuntary
126690371 12669037 Muscle rupture
126690371 12669037 Myoglobinuria
126690371 12669037 Polyuria

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found