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
109532305 10953230 5 F 20160901 20150325 20160907 EXP JP-SA-2015SA035905 AVENTIS NISHIHAMA K, MAKI K, OKANO Y, HASHIMOTO R, HOTTA Y, UEMURA M ET AL. A CASE OF TYPE 2 DIABETES MELLITUS WITH METFORMIN-ASSOCIATED LACTIC ACIDOSIS INITIALLY PRESENTING THE APPEARANCE OF A SULFONYLUREA-RELATED HYPOGLYCEMIC ATTACK. ACUTE MEDICINE AND SURGERY 2016. DOI: 10.1002/AMS2.233 64.00 YR A F Y 77.20000 KG 20160907 MD JP JP

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
109532305 10953230 1 PS GLIMEPIRIDE. GLIMEPIRIDE 1 Oral U UNK 20496 1 MG QD
109532305 10953230 2 SS VOGLIBOSE VOGLIBOSE 1 Oral U UNK 0 .9 MG QD
109532305 10953230 3 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Oral U UNK 0 2250 MG QD
109532305 10953230 4 SS CANDESARTAN CILEXETIL. CANDESARTAN CILEXETIL 1 Unknown U UNK 0 8 MG QD
109532305 10953230 5 SS OLMESARTAN OLMESARTAN 1 Unknown U UNK 0 20 MG QD
109532305 10953230 6 C EXENATIDE EXENATIDE 1 0 20 UG QD
109532305 10953230 7 C AMLODIPINE AMLODIPINE BESYLATE 1 0 5 MG QD
109532305 10953230 8 C ROSUVASTATIN. ROSUVASTATIN 1 0 2.5 MG QD
109532305 10953230 9 C TOCOPHEROL TOCOPHEROL 1 0 600 MG QD
109532305 10953230 10 C POLAPREZINC POLAPREZINC 1 0 150 MG QD
109532305 10953230 11 C CEFTRIAXONE. CEFTRIAXONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109532305 10953230 1 Type 2 diabetes mellitus
109532305 10953230 2 Type 2 diabetes mellitus
109532305 10953230 3 Type 2 diabetes mellitus
109532305 10953230 4 Hypertension
109532305 10953230 5 Hypertension
109532305 10953230 6 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
109532305 10953230 HO
109532305 10953230 LT
109532305 10953230 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109532305 10953230 Acute kidney injury
109532305 10953230 Anion gap increased
109532305 10953230 Base excess decreased
109532305 10953230 Blood bicarbonate decreased
109532305 10953230 Blood creatinine increased
109532305 10953230 Blood lactic acid increased
109532305 10953230 Blood pH decreased
109532305 10953230 Blood urea increased
109532305 10953230 Blood uric acid increased
109532305 10953230 C-reactive protein increased
109532305 10953230 Condition aggravated
109532305 10953230 Costovertebral angle tenderness
109532305 10953230 Decreased appetite
109532305 10953230 Dehydration
109532305 10953230 Drug level increased
109532305 10953230 Fatigue
109532305 10953230 Hypoglycaemia
109532305 10953230 Lactic acidosis
109532305 10953230 Metabolic acidosis
109532305 10953230 Oedema peripheral
109532305 10953230 PO2 decreased
109532305 10953230 Peripheral circulatory failure
109532305 10953230 Renal impairment

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

no results found

Therapies reported

no results found