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
125229481 12522948 1 I 2008 20160621 20160701 20160701 EXP BR-009507513-1606BRA011066 MERCK 51.00 YR F Y 58.00000 KG 20160701 CN BR BR

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
125229481 12522948 1 PS VYTORIN EZETIMIBESIMVASTATIN 1 Oral UNK 21687 TABLET
125229481 12522948 2 C CELESTAMINE BETAMETHASONEDEXCHLORPHENIRAMINE MALEATE 1 Oral 1 TABLET, Q12H, WHENEVER IS NECESSARY U 0 1 DF TABLET Q12H
125229481 12522948 3 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 40 MG IN FASTING U 0 40 MG
125229481 12522948 4 C MOTILIUM DOMPERIDONE 1 WHENEVER IS NECESSARY U 0
125229481 12522948 5 C DUCAMARA 30CH 2 U 0
125229481 12522948 6 C ACONITUM NATELLLUS 30CH 2 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125229481 12522948 1 Hypertension
125229481 12522948 2 Hypersensitivity
125229481 12522948 3 Gastrooesophageal reflux disease
125229481 12522948 4 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
125229481 12522948 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125229481 12522948 Allergic respiratory symptom
125229481 12522948 Gastrooesophageal reflux disease
125229481 12522948 Hysterectomy
125229481 12522948 Oophorectomy
125229481 12522948 Oral herpes
125229481 12522948 Product use issue
125229481 12522948 Sudden hearing loss

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
125229481 12522948 1 2008 0