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
125356991 12535699 1 I 20160627 20160707 20160707 EXP CZ-PAR PHARMACEUTICAL COMPANIES-2016SCPR015611 PAR POLAK P., HUSA P., KUBESOVA H.M.. SEVERE OSTEOPOROSIS - THE STORY OF CHRONIC MEDICATION-RELATED HYPONATREMIA. VNITRNI LEKARSTVI. 2016;62(2):152-156 0.00 Y 0.00000 20160707 OT CZ CZ

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
125356991 12535699 1 PS AMILORIDE HCL AMILORIDE HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN U U 70346
125356991 12535699 2 SS THIAZIDES UNSPECIFIED INGREDIENT 1 Unknown UNK UNK, UNKNOWN U U 0
125356991 12535699 3 SS INDAPAMIDE. INDAPAMIDE 1 Unknown UNK UNK, UNKNOWN U U 0
125356991 12535699 4 SS TRAZODONE TRAZODONE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125356991 12535699 1 Hypertension
125356991 12535699 2 Hypertension
125356991 12535699 3 Hypertension
125356991 12535699 4 Antidepressant therapy

Outcome of event

Event ID CASEID OUTC COD
125356991 12535699 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125356991 12535699 Hyponatraemia
125356991 12535699 Multiple fractures
125356991 12535699 Osteoporosis

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

no results found

Therapies reported

no results found