The Safety Rates Drug Report

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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
124981022 12498102 2 F 2016 20160704 20160626 20160713 EXP GB-MYLANLABS-2016M1025166 MYLAN 0.00 Y 0.00000 20160713 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
124981022 12498102 1 PS ONDANSETRON ONDANSETRON 1 UNK U U 76930
124981022 12498102 2 SS NEULASTA PEGFILGRASTIM 1 Subcutaneous 6 MG, UNK (6 MG, 24 HOURS AFTER CHEMOTHERAPY) U U 0 6 MG
124981022 12498102 3 SS APREPITANT. APREPITANT 1 Oral 80 MG, QD (80 MG, ONCE A DAY (TAKEN ON DAY 2 AND 3 AFTER CHEMOTHERAPY) U U 0 80 MG QD
124981022 12498102 4 SS FLUOROURACIL. FLUOROURACIL 1 UNK (UNK, EVERY 3 WEEKS (CYCLICAL) U U 0
124981022 12498102 5 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 2 MG, QD (2 MG, ONCE DAILY, 3 DAYS) U U 0 2 MG QD
124981022 12498102 6 SS DOCETAXEL. DOCETAXEL 1 UNK (3 CYCLES) U U 0
124981022 12498102 7 SS LEVOMEPROMAZINE LEVOMEPROMAZINE 1 UNK (UNK) U U 0
124981022 12498102 8 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 UNK (UNK) U U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
124981022 12498102 HO
124981022 12498102 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124981022 12498102 Arthralgia
124981022 12498102 Constipation
124981022 12498102 Decreased appetite
124981022 12498102 Deep vein thrombosis
124981022 12498102 Fatigue
124981022 12498102 Oral pain
124981022 12498102 Pain
124981022 12498102 Pain in extremity
124981022 12498102 Peripheral swelling
124981022 12498102 Vascular pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found