The Safety Rates Drug Report

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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
125522612 12552261 2 F 20160707 20160713 20160721 EXP ZA-CONCORDIA PHARMACEUTICALS INC.-GSH201607-003560 CONCORDIA MOUTON J,NJUGUNA C,KRAMER N,STEWART A,MEHTA U,COHEN K. ADVERSE DRUG REACTIONS CAUSING ADMISSION TO MEDICAL WARDS: A CROSS-SECTIONAL SURVEY AT 4 HOSPITALS IN SOUTH AFRICA. MEDICINE 2016 MAY;95(19):1-10. 56.00 YR F Y 0.00000 20160721 OT ZA ZA

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
125522612 12552261 1 SS HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 Unknown U 0
125522612 12552261 2 PS Metoprolol Hydrochlorothiazide HYDROCHLOROTHIAZIDEMETOPROLOL TARTRATE 1 Unknown U 21956
125522612 12552261 3 SS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown U 0
125522612 12552261 4 SS ATENOLOL. ATENOLOL 1 Unknown U 0
125522612 12552261 5 SS Enalapril ENALAPRIL 1 Unknown U 0
125522612 12552261 6 SS FUROSEMIDE. FUROSEMIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125522612 12552261 1 Product used for unknown indication
125522612 12552261 2 Product used for unknown indication
125522612 12552261 3 Product used for unknown indication
125522612 12552261 4 Product used for unknown indication
125522612 12552261 5 Product used for unknown indication
125522612 12552261 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125522612 12552261 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125522612 12552261 Renal impairment

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

no results found

Therapies reported

no results found