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
127081481 12708148 1 I 20121128 20121215 20160901 20160901 EXP US-PFIZER INC-2012318763 PFIZER 71.00 YR M Y 84.00000 KG 20160901 MD 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
127081481 12708148 1 PS CELECOXIB. CELECOXIB 1 Oral UNK 20998 CAPSULE, HARD
127081481 12708148 2 SS CELECOXIB. CELECOXIB 1 20998 CAPSULE, HARD
127081481 12708148 3 SS FUROSEMIDE. FUROSEMIDE 1 Oral 20 MG, 1X/DAY Y 18667 20 MG QD
127081481 12708148 4 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral UNK, 1X/DAY 0 QD
127081481 12708148 5 C GLUCOSAMINE CHONDROITIN PM 2 UNK 0
127081481 12708148 6 C TAMSULOSIN TAMSULOSIN 1 UNK 0
127081481 12708148 7 C PLAVIX CLOPIDOGREL BISULFATE 1 UNK 0
127081481 12708148 8 C SOLIFENACIN SUCCINATE. SOLIFENACIN SUCCINATE 1 UNK 0
127081481 12708148 9 C DOCUSATE SODIUM. DOCUSATE SODIUM 1 UNK 0
127081481 12708148 10 C CALCIUM CARBONATE W/VITAMIN D 2 UNK 0
127081481 12708148 11 C CALCIUM CARBONATE W/VITAMIN D 2 0
127081481 12708148 12 C MAGNESIUM MAGNESIUM 1 UNK 0
127081481 12708148 13 C GLIPIZIDE. GLIPIZIDE 1 UNK 0
127081481 12708148 14 C LANTUS INSULIN GLARGINE 1 UNK 0
127081481 12708148 15 C SIMVASTATIN. SIMVASTATIN 1 UNK 0
127081481 12708148 16 C OMEPRAZOLE. OMEPRAZOLE 1 UNK 0
127081481 12708148 17 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 UNK 0
127081481 12708148 18 C LISINOPRIL. LISINOPRIL 1 UNK 0
127081481 12708148 19 C OMEGA 3 FATTY ACIDS OMEGA-3 FATTY ACIDS 1 UNK 0
127081481 12708148 20 C FERROUS SULFATE. FERROUS SULFATE 1 UNK 0
127081481 12708148 21 C ACETYLSALICYLIC ACID ASPIRIN 1 UNK 0
127081481 12708148 22 C TRAMADOL. TRAMADOL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127081481 12708148 1 Osteoarthritis
127081481 12708148 2 Rheumatoid arthritis
127081481 12708148 3 Oedema
127081481 12708148 4 Prophylaxis
127081481 12708148 5 Osteoarthritis
127081481 12708148 6 Benign prostatic hyperplasia
127081481 12708148 7 Transient ischaemic attack
127081481 12708148 8 Hypertonic bladder
127081481 12708148 9 Constipation
127081481 12708148 10 Supplementation therapy
127081481 12708148 11 Muscle spasms
127081481 12708148 12 Muscle spasms
127081481 12708148 13 Type 2 diabetes mellitus
127081481 12708148 14 Type 2 diabetes mellitus
127081481 12708148 15 Hypertriglyceridaemia
127081481 12708148 16 Gastrooesophageal reflux disease
127081481 12708148 17 Hypertension
127081481 12708148 18 Hypertension
127081481 12708148 19 Hypertriglyceridaemia
127081481 12708148 20 Anaemia
127081481 12708148 21 Transient ischaemic attack
127081481 12708148 22 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
127081481 12708148 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127081481 12708148 Syncope

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
127081481 12708148 1 20120907 20121107 0
127081481 12708148 3 2000 20121128 0
127081481 12708148 4 20120907 0
127081481 12708148 5 1979 0
127081481 12708148 6 2005 0
127081481 12708148 7 2000 0
127081481 12708148 8 2007 0
127081481 12708148 9 2003 0
127081481 12708148 10 1996 0
127081481 12708148 12 1998 0
127081481 12708148 13 2004 0
127081481 12708148 14 2006 0
127081481 12708148 15 2002 0
127081481 12708148 16 1982 0
127081481 12708148 17 2004 0
127081481 12708148 18 2004 0
127081481 12708148 19 1999 0
127081481 12708148 20 2002 0
127081481 12708148 21 2000 0
127081481 12708148 22 20120913 0