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
125643881 12564388 1 I 20160715 20160718 20160718 EXP US-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00321 SCIEGEN 46.00 YR M Y 0.00000 20160718 MD 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
125643881 12564388 1 PS Hydrochlorothiazide Tablets HYDROCHLOROTHIAZIDE 1 Unknown UNK U U 203018 TABLET
125643881 12564388 2 SS CALCIUM CARBONATE. CALCIUM CARBONATE 1 Unknown UNK U U 0
125643881 12564388 3 SS NSAIDS UNSPECIFIED INGREDIENT 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125643881 12564388 1 Hypertension
125643881 12564388 2 Product used for unknown indication
125643881 12564388 3 Arthritis

Outcome of event

Event ID CASEID OUTC COD
125643881 12564388 OT
125643881 12564388 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125643881 12564388 Abdominal pain upper
125643881 12564388 Abdominal tenderness
125643881 12564388 Acute kidney injury
125643881 12564388 Bundle branch block left
125643881 12564388 Chest pain
125643881 12564388 Electrocardiogram ST segment elevation
125643881 12564388 Hypercalcaemia
125643881 12564388 Milk-alkali syndrome
125643881 12564388 Nausea
125643881 12564388 Vomiting

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

no results found

Therapies reported

no results found