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
127064181 12706418 1 I 20160818 20160901 20160901 PER US-PFIZER INC-2016395679 PFIZER 47.00 YR F Y 63.39000 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
127064181 12706418 1 PS DOXORUBICIN HCL DOXORUBICIN HYDROCHLORIDE 1 UNK U 50467
127064181 12706418 2 SS CALCIUM FOLINATE LEUCOVORIN CALCIUM 1 UNK U 8107
127064181 12706418 3 SS CYTARABINE. CYTARABINE 1 UNK U 71868
127064181 12706418 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK U 11719
127064181 12706418 5 SS METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 UNK U 40664 POWDER FOR INJECTION
127064181 12706418 6 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 UNK U 71484
127064181 12706418 7 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK U 0
127064181 12706418 8 SS DEXAMETHASONE. DEXAMETHASONE 1 UNK U 0
127064181 12706418 9 SS NILOTINIB NILOTINIB 1 UNK U 0
127064181 12706418 10 SS DASATINIB DASATINIB 1 UNK U 0
127064181 12706418 11 SS PONATINIB PONATINIB 1 UNK U 0
127064181 12706418 12 C ACYCLOVIR. ACYCLOVIR 1 40 MG, 3X/DAY 0 40 MG TID
127064181 12706418 13 C CIPROFLOXACIN. CIPROFLOXACIN 1 500 MG, 2X/DAY 0 500 MG BID
127064181 12706418 14 C FLUCONAZOLE. FLUCONAZOLE 1 400 MG, DAILY 0 400 MG
127064181 12706418 15 C BACTRIM DS SULFAMETHOXAZOLETRIMETHOPRIM 1 1 DF, 2X/DAY(BID ON MONDAYS AND THURSDAY) 0 1 DF TABLET BID
127064181 12706418 16 C AMITRIPTYLINE AMITRIPTYLINE 1 25 MG, DAILY 0 25 MG
127064181 12706418 17 C FAMOTIDINE. FAMOTIDINE 1 40 MG, 1X/DAY 0 40 MG QD
127064181 12706418 18 C COMPAZINE PROCHLORPERAZINE MALEATE 1 10 MG, AS NEEDED 0 10 MG
127064181 12706418 19 C COMPAZINE PROCHLORPERAZINE MALEATE 1 0
127064181 12706418 20 C AMLODIPINE AMLODIPINE BESYLATE 1 5 MG, 1X/DAY 0 5 MG QD
127064181 12706418 21 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 10 MG, 1X/DAY 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127064181 12706418 1 Acute lymphocytic leukaemia
127064181 12706418 2 Acute lymphocytic leukaemia
127064181 12706418 3 Acute lymphocytic leukaemia
127064181 12706418 4 Acute lymphocytic leukaemia
127064181 12706418 5 Acute lymphocytic leukaemia
127064181 12706418 6 Acute lymphocytic leukaemia
127064181 12706418 7 Acute lymphocytic leukaemia
127064181 12706418 8 Acute lymphocytic leukaemia
127064181 12706418 9 Acute lymphocytic leukaemia
127064181 12706418 10 Acute lymphocytic leukaemia
127064181 12706418 11 Acute lymphocytic leukaemia
127064181 12706418 18 Nausea
127064181 12706418 19 Vomiting

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127064181 12706418 Acute lymphocytic leukaemia
127064181 12706418 Disease progression

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
127064181 12706418 1 20160505 0
127064181 12706418 2 20160505 0
127064181 12706418 3 20160505 0
127064181 12706418 4 20160505 0
127064181 12706418 5 20160505 0
127064181 12706418 6 20160505 0
127064181 12706418 7 20160505 0
127064181 12706418 8 20160505 0
127064181 12706418 9 20160505 0
127064181 12706418 10 20160505 0
127064181 12706418 11 20160617 0