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
126561511 12656151 1 I 2016 20160810 20160816 20160816 EXP US-PFIZER INC-2016383365 PFIZER 65.00 YR F Y 92.30000 KG 20160816 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
126561511 12656151 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY 20753 25 MG COATED TABLET QD
126561511 12656151 2 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 1 MG, 2X/DAY 0 1 MG BID
126561511 12656151 3 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 250 MG, 2X/DAY 0 250 MG BID
126561511 12656151 4 C METOPROLOL. METOPROLOL 1 100 MG, 2X/DAY 0 100 MG BID
126561511 12656151 5 C HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 UNK, 3X/DAY 0 TID
126561511 12656151 6 C CLONIDINE. CLONIDINE 1 0.2 MG, 3X/DAY 0 .2 MG TID
126561511 12656151 7 C LOPRESSOR METOPROLOL TARTRATE 1 UNK 0
126561511 12656151 8 C Gliburide 2 5 MG, 2X/DAY 0 5 MG BID
126561511 12656151 9 C LANTUS INSULIN GLARGINE 1 25 IU, 1X/DAY 0 25 IU QD
126561511 12656151 10 C ASPIRIN /00002701/ ASPIRIN 1 81 MG, 1X/DAY 0 81 MG QD
126561511 12656151 11 C PROTONIX PANTOPRAZOLE SODIUM 1 40 MG, 1X/DAY 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126561511 12656151 1 Breast cancer
126561511 12656151 2 Prophylaxis against transplant rejection
126561511 12656151 3 Prophylaxis against transplant rejection
126561511 12656151 4 Hypertension
126561511 12656151 5 Hypertension
126561511 12656151 6 Hypertension
126561511 12656151 7 Blood cholesterol abnormal
126561511 12656151 8 Diabetes mellitus
126561511 12656151 9 Diabetes mellitus
126561511 12656151 10 Cardiac disorder
126561511 12656151 11 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
126561511 12656151 OT
126561511 12656151 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126561511 12656151 Blood creatinine increased
126561511 12656151 Blood magnesium decreased
126561511 12656151 Blood potassium increased
126561511 12656151 Depression
126561511 12656151 Dyspnoea
126561511 12656151 Pulmonary oedema
126561511 12656151 Respiratory tract infection

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
126561511 12656151 1 201505 0
126561511 12656151 2 200911 0
126561511 12656151 3 2010 0