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
117166962 11716696 2 F 201101 20160718 20151109 20160725 EXP US-DSJP-DSU-2015-120851 DAIICHI 0.00 Y 0.00000 20160725 CN 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
117166962 11716696 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 20 MG, QD Y UNKNOWN 21286 20 MG TABLET QD
117166962 11716696 2 SS BENICAR OLMESARTAN MEDOXOMIL 1 Y 21286 TABLET
117166962 11716696 3 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 40MG/25MG, BID Y UNKNOWN 0 1 DF FILM-COATED TABLET BID
117166962 11716696 4 SS BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Y 0 FILM-COATED TABLET
117166962 11716696 5 C LASIX FUROSEMIDE 1 20 MG, PRN 0 20 MG
117166962 11716696 6 C OXYCODONE OXYCODONE 1 15 MG, UNK 0 15 MG
117166962 11716696 7 C OXYCODONE HYDROCHLORIDE. OXYCODONE HYDROCHLORIDE 1 30 MG, QID 0 30 MG QID
117166962 11716696 8 C OPANA OXYMORPHONE HYDROCHLORIDE 1 UNK 0
117166962 11716696 9 C OPANA OXYMORPHONE HYDROCHLORIDE 1 0
117166962 11716696 10 C IBUPROFEN. IBUPROFEN 1 UNK 0
117166962 11716696 11 C IBUPROFEN. IBUPROFEN 1 0
117166962 11716696 12 C VALISONE BETAMETHASONE VALERATE 1 UNK 0 CREAM
117166962 11716696 13 C VALISONE BETAMETHASONE VALERATE 1 0 CREAM
117166962 11716696 14 C PREVACID LANSOPRAZOLE 1 30 MG, UNK 0 30 MG
117166962 11716696 15 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 40 MG, BID 0 40 MG BID
117166962 11716696 16 C CEPHALEXINE CEPHALEXIN 1 UNK 0
117166962 11716696 17 C MAGNESIUM MAGNESIUM 1 UNK 0
117166962 11716696 18 C POTASSIUM CL POTASSIUM CHLORIDE 1 UNK 0
117166962 11716696 19 C FOLIC ACID. FOLIC ACID 1 UNK 0
117166962 11716696 20 C LACTULOSE. LACTULOSE 1 UNK 0
117166962 11716696 21 C MULTIVITAMIN /00097801/ VITAMINS 1 UNK 0
117166962 11716696 22 C THIAMINE. THIAMINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117166962 11716696 1 Hypertension
117166962 11716696 2 Headache
117166962 11716696 3 Headache
117166962 11716696 4 Hypertension
117166962 11716696 5 Oedema peripheral
117166962 11716696 6 Back pain
117166962 11716696 7 Pain
117166962 11716696 8 Back pain
117166962 11716696 9 Pain
117166962 11716696 10 Intervertebral disc degeneration
117166962 11716696 11 Back pain
117166962 11716696 12 Dermatitis
117166962 11716696 13 Pruritus
117166962 11716696 14 Gastrooesophageal reflux disease
117166962 11716696 15 Pain
117166962 11716696 16 Product used for unknown indication
117166962 11716696 17 Product used for unknown indication
117166962 11716696 18 Product used for unknown indication
117166962 11716696 19 Product used for unknown indication
117166962 11716696 20 Product used for unknown indication
117166962 11716696 21 Product used for unknown indication
117166962 11716696 22 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117166962 11716696 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117166962 11716696 Acute kidney injury
117166962 11716696 Adenoma benign
117166962 11716696 Large intestine polyp
117166962 11716696 Malabsorption
117166962 11716696 Muscle fatigue
117166962 11716696 Poverty of speech
117166962 11716696 Shock

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
117166962 11716696 1 200206 200411 0
117166962 11716696 3 200411 201204 0
117166962 11716696 5 201202 0
117166962 11716696 8 201105 201203 0
117166962 11716696 12 201108 201201 0
117166962 11716696 14 2006 2009 0
117166962 11716696 21 201202 201203 0