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
127252491 12725249 1 I 20140605 20140612 20160908 20160908 EXP US-PFIZER INC-2014163007 PFIZER 59.00 YR F Y 39.00000 KG 20160908 OT 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
127252491 12725249 1 PS CYTARABINE. CYTARABINE 1 Intravenous (not otherwise specified) 210 MG, CONTINUOUS INFUSION ON DAYS 1-7 71868 210 MG
127252491 12725249 2 SS CYTARABINE. CYTARABINE 1 Intravenous (not otherwise specified) 2090 MG, CONTINUOUS INFUSION ON DAYS 1-7 71868 2090 MG
127252491 12725249 3 SS PF-04449913 GLASDEGIB 1 Oral 100 MG, ONCE DAILY CONTINUOUS 0 100 MG TABLET QD
127252491 12725249 4 SS DAUNORUBICIN DAUNORUBICIN 1 Intravenous (not otherwise specified) 127 MG, CYCLIC, DAY 1-3 0 127 MG
127252491 12725249 5 C ACYCLOVIR. ACYCLOVIR 1 UNK 0
127252491 12725249 6 C MAALOX ANTACID ALUMINUM HYDROXIDEDIMETHICONEMAGNESIUM HYDROXIDE 1 UNK 0
127252491 12725249 7 C CHOLECALCIFEROL CHOLECALCIFEROL 1 UNK 0
127252491 12725249 8 C CELEXA CITALOPRAM HYDROBROMIDE 1 UNK 0
127252491 12725249 9 C HEPARIN FLUSH HEPARIN SODIUM 1 UNK 0
127252491 12725249 10 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK 0
127252491 12725249 11 C METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 UNK 0
127252491 12725249 12 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 UNK 0
127252491 12725249 13 C VANCOMYCIN VANCOMYCIN 1 UNK 0
127252491 12725249 14 C LEVAQUIN LEVOFLOXACIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127252491 12725249 1 Acute myeloid leukaemia
127252491 12725249 3 Acute myeloid leukaemia
127252491 12725249 4 Acute myeloid leukaemia
127252491 12725249 5 Prophylaxis
127252491 12725249 6 Gastrooesophageal reflux disease
127252491 12725249 7 Supplementation therapy
127252491 12725249 8 Depression
127252491 12725249 9 Catheter management
127252491 12725249 10 Hypothyroidism
127252491 12725249 11 Hypertension
127252491 12725249 12 Nausea
127252491 12725249 13 Clostridium difficile infection
127252491 12725249 14 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127252491 12725249 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127252491 12725249 Abdominal pain
127252491 12725249 Confusional state
127252491 12725249 Diarrhoea
127252491 12725249 Febrile neutropenia
127252491 12725249 Hyponatraemia

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
127252491 12725249 1 20140227 20140305 0
127252491 12725249 2 20140527 0
127252491 12725249 3 20140224 0
127252491 12725249 4 20140227 20140301 0