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
125515431 12551543 1 I 20160628 20160713 20160713 EXP US-CIPLA LTD.-2016US09389 CIPLA SPIGEL DR, HAINSWORTH JD, SHIPLEY DL, ERVIN TJ, KOHLER PC, LUBINER ET ET AL.,. A RANDOMIZED PHASE II TRIAL OF PEMETREXED/GEMCITABINE/BEVACIZUMAB OR PEMETREXED/CARBOPLATIN/BEVACIZUMAB IN THE FIRST-LINE TREATMENT OF ELDERLY PATIENTS WITH ADVANCED NON-SMALL CELL LUNG CANCER. J THORAC ONCOL. 2012;7:196 TO 202 0.00 Y 0.00000 20160713 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
125515431 12551543 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1500 MG/M2,DAYS 1 AND 15 OF EACH 28-DAY CYCLE U U 78759 1500 MG/M**2
125515431 12551543 2 SS Pemetrexed PEMETREXED 1 Intravenous (not otherwise specified) 500 MG/M2, DAYS 1 AND 15 OF EACH 28-DAY CYCLE U U 0 500 MG/M**2
125515431 12551543 3 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) 10 MG/KG, DAYS 1 AND 15 OF EACH 28-DAY CYCLE U U 0 10 MG/KG
125515431 12551543 4 C FOLIC ACID. FOLIC ACID 1 Oral 300 -1000 MICROGRAMS U U 0
125515431 12551543 5 C VITAMIN B12 CYANOCOBALAMIN 1 Intramuscular 1000 ?G, UNK U U 0 1000 UG INJECTION
125515431 12551543 6 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U U 0
125515431 12551543 7 C LEUCOVORIN. LEUCOVORIN 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125515431 12551543 1 Non-small cell lung cancer
125515431 12551543 2 Non-small cell lung cancer
125515431 12551543 3 Non-small cell lung cancer
125515431 12551543 6 Premedication
125515431 12551543 7 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125515431 12551543 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125515431 12551543 Dyspnoea

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

no results found

Therapies reported

no results found