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
125519801 12551980 1 I 20160708 20160713 20160713 EXP CA-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00300 SCIEGEN 79.00 YR M Y 0.00000 20160713 MD CA CA

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
125519801 12551980 1 PS Olmesartan Medoxomil tablets 5 mg, 20 mg, 40 mg OLMESARTAN MEDOXOMIL 1 Unknown 40 MG, QD Y U 208130 40 MG TABLET
125519801 12551980 2 SS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 5 MG, UNK U 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125519801 12551980 1 Hypertension
125519801 12551980 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125519801 12551980 HO
125519801 12551980 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125519801 12551980 Abdominal pain
125519801 12551980 Acute kidney injury
125519801 12551980 Dehydration
125519801 12551980 Diarrhoea
125519801 12551980 Gastrointestinal disorder
125519801 12551980 Hypotension
125519801 12551980 Hypovolaemia
125519801 12551980 Metabolic acidosis
125519801 12551980 Nausea
125519801 12551980 Vomiting
125519801 12551980 Weight decreased

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

no results found

Therapies reported

no results found