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
80468075 8046807 5 F 20130916 20110721 20130930 EXP GB-RANBAXY-2011R1-45900 RANBAXY 31.00 YR F Y 0.00000 20130930 OT GB GB

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
80468075 8046807 1 PS Ramipril 1 UNKNOWN 10 MG, 1/1 DAY D 78849 10 MG
80468075 8046807 2 SS Bendroflumethiazide 1 UNKNOWN 5 MG, QD D 0 5 MG
80468075 8046807 3 SS Bendroflumethiazide 1 UNKNOWN 2.5 MG, QD INCREASED TO 5 MG D 0 2.5 MG
80468075 8046807 4 C Mesalazine 1 UNKNOWN 800 MG, 2/1 DAYS U 0 800 MG Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
80468075 8046807 1 Hypertension
80468075 8046807 2 Hypertension
80468075 8046807 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
80468075 8046807 LT
80468075 8046807 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
80468075 8046807 Asthenia
80468075 8046807 Blood osmolarity abnormal
80468075 8046807 Blood potassium abnormal
80468075 8046807 Blood pressure abnormal
80468075 8046807 Blood sodium abnormal
80468075 8046807 Cardiac arrest
80468075 8046807 Confusional state
80468075 8046807 Convulsion
80468075 8046807 Hypokalaemia
80468075 8046807 Hyponatraemia
80468075 8046807 Palpitations
80468075 8046807 Paraesthesia
80468075 8046807 Presyncope
80468075 8046807 Urine sodium abnormal
80468075 8046807 Ventricular extrasystoles
80468075 8046807 Vomiting
80468075 8046807 Water intoxication

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

no results found

Therapies reported

no results found