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
126739711 12673971 1 I 20120723 20121105 20160822 20160822 EXP GB-PFIZER INC-2012275806 PFIZER 5.00 YR M Y 15.25000 KG 20160822 OT GB GB

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
126739711 12673971 1 PS DOXORUBICIN HCL DOXORUBICIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) 20 MG, CYCLIC (DAY 1 AND 2 EACH CYCLE) 50467 20 MG
126739711 12673971 2 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 Intravenous (not otherwise specified) 1 MG, WEEKLY .429 MG UNK 71484 1 MG /wk
126739711 12673971 3 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 Intravenous (not otherwise specified) UNK .429 MG 71484
126739711 12673971 4 SS IFOSFAMIDE. IFOSFAMIDE 1 Intravenous (not otherwise specified) 2 G, DAY 1 AND 2 OF EACH CYCLE 0 2 G
126739711 12673971 5 SS DACTINOMYCIN DACTINOMYCIN 1 Intravenous (not otherwise specified) 1 MG, ONE PER ONE CYCLE, CYCLICAL 0 1 MG
126739711 12673971 6 C COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 920 MG, UNK 0 920 MG
126739711 12673971 7 C MOVICOL POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE 1 1, UNK 0
126739711 12673971 8 C PARACETAMOL ACETAMINOPHEN 1 960 MG, UNK 0 960 MG
126739711 12673971 9 C PARACETAMOL ACETAMINOPHEN 1 240 MG, UNK 0 240 MG
126739711 12673971 10 C PARACETAMOL ACETAMINOPHEN 1 1 G, UNK 0 1 G
126739711 12673971 11 C ORAMORPH MORPHINE SULFATE 1 12 MG, UNK 0 12 MG
126739711 12673971 12 C CHLORHEXIDINE CHLORHEXIDINE 1 UNK 0 MOUTH WASH
126739711 12673971 13 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 7.5 MG, UNK 0 7.5 MG
126739711 12673971 14 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 980 MG, UNK 0 980 MG
126739711 12673971 15 C GRANISETRON GRANISETRON 1 960 MG, UNK 0 960 MG
126739711 12673971 16 C GRANISETRON GRANISETRON 1 1.28 MG, UNK 0 1.28 MG
126739711 12673971 17 C ONDANSETRON ONDANSETRON 1 7.5 MG, UNK 0 7.5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126739711 12673971 1 Neoplasm malignant
126739711 12673971 2 Neoplasm malignant
126739711 12673971 4 Neoplasm malignant
126739711 12673971 5 Neoplasm malignant
126739711 12673971 6 Product used for unknown indication
126739711 12673971 7 Product used for unknown indication
126739711 12673971 8 Product used for unknown indication
126739711 12673971 11 Product used for unknown indication
126739711 12673971 12 Product used for unknown indication
126739711 12673971 13 Product used for unknown indication
126739711 12673971 15 Product used for unknown indication
126739711 12673971 17 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126739711 12673971 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126739711 12673971 Febrile neutropenia
126739711 12673971 Hypophagia

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
126739711 12673971 1 20120721 0
126739711 12673971 2 20120720 0
126739711 12673971 3 20120816 0
126739711 12673971 4 20120720 0
126739711 12673971 5 20120720 0
126739711 12673971 6 20120724 0
126739711 12673971 7 20120730 0
126739711 12673971 8 20120705 0
126739711 12673971 10 20121208 0
126739711 12673971 11 20120725 0
126739711 12673971 13 20120720 0
126739711 12673971 14 20121207 0
126739711 12673971 15 20120723 0
126739711 12673971 17 20121207 0