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
126497991 12649799 1 I 2014 20160728 20160812 20160812 EXP US-009507513-1608USA007151 MERCK 70.58 YR F Y 65.31000 KG 20160812 CN US US

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
126497991 12649799 1 SS OLMESARTAN MEDOXOMIL. OLMESARTAN MEDOXOMIL 1 Oral 40 MG, QD 0 40 MG TABLET QD
126497991 12649799 2 PS COZAAR LOSARTAN POTASSIUM 1 Unknown UNKNOWN Y 20386 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126497991 12649799 1 Hypertension
126497991 12649799 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126497991 12649799 HO
126497991 12649799 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126497991 12649799 Abdominal distension
126497991 12649799 Alopecia
126497991 12649799 Asthma
126497991 12649799 Atrial fibrillation
126497991 12649799 Back pain
126497991 12649799 Brain injury
126497991 12649799 Cerebrovascular accident
126497991 12649799 Drug ineffective
126497991 12649799 Generalised oedema
126497991 12649799 Inflammation
126497991 12649799 Musculoskeletal disorder
126497991 12649799 Treatment noncompliance
126497991 12649799 Vomiting
126497991 12649799 Weight decreased

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
126497991 12649799 1 20110101 201509 0
126497991 12649799 2 2015 2016 0