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
125515661 12551566 1 I 20130507 20160713 20160713 EXP US-CIPLA LTD.-2013US00508 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 (1):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
125515661 12551566 1 PS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) AUC 5, ON DAY 1, EVENRY 21 DAYS 0
125515661 12551566 2 SS Pemetrexed PEMETREXED 1 Intravenous (not otherwise specified) 500 MG/M2, ON DAY 1, EVERY 21 DAYS N 0 500 MG/M**2
125515661 12551566 3 SS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) 15 MG/KG, ON DAY 1, EVERY 21 DAYS 0 15 MG/KG
125515661 12551566 4 C FOLIC ACID. FOLIC ACID 1 Oral 350 TO 1000 MICROGRAMS, DAILY U U 0
125515661 12551566 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
125515661 12551566 6 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U U 0
125515661 12551566 7 C LEUCOVORIN. LEUCOVORIN 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125515661 12551566 1 Non-small cell lung cancer
125515661 12551566 2 Non-small cell lung cancer
125515661 12551566 3 Non-small cell lung cancer
125515661 12551566 6 Premedication
125515661 12551566 7 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125515661 12551566 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125515661 12551566 Sepsis

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

no results found

Therapies reported

no results found