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
125522631 12552263 1 I 20160628 20160713 20160713 EXP US-CIPLA LTD.-2016US09375 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. JOURNAL OF THORACIC ONCOLOGY. 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
125522631 12552263 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1500 MG/M2, ON DAYS 1 AND 15 OF EACH 28-DAY CYCLE 78759 1500 MG/M**2
125522631 12552263 2 SS Pemetrexed PEMETREXED 1 Intravenous (not otherwise specified) 500 MG/M2,ON DAYS 1 AND 15 OF EACH 28-DAY CYCLE 0 500 MG/M**2
125522631 12552263 3 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) 10 MG/KG,ON DAYS 1 AND 15 OF EACH 28-DAY CYCLE 0 10 MG/KG
125522631 12552263 4 C FOLIC ACID. FOLIC ACID 1 Oral 350 TO 1000 MCG, DAILY U U 0
125522631 12552263 5 C VITAMIN B12 CYANOCOBALAMIN 1 Intramuscular 1000 MCG, EVERY 9 WEEKS UNTIL 3 WEEKS AFTER THE LAST DOSE OF PEMETREXED U U 0 1000 UG
125522631 12552263 6 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U U 0
125522631 12552263 7 C LEUCOVORIN. LEUCOVORIN 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125522631 12552263 1 Non-small cell lung cancer
125522631 12552263 2 Non-small cell lung cancer
125522631 12552263 3 Non-small cell lung cancer stage IV
125522631 12552263 6 Premedication
125522631 12552263 7 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125522631 12552263 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125522631 12552263 Thrombocytopenia

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

no results found

Therapies reported

no results found