The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6810139 7428888 F 6810139-9 20100617 20100625 20100630 EXP PT-CELGENEUS-130-C5013-10061828 CELGENEUS 79 YR M Y 67 KG 20100630 OT 20100621 PORTUGAL

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6810139 1014006354 PS CC-5013 2 ORAL 60100
6810139 1014006355 SS DEXAMETHASONE 2 UNKNOWN
6810139 1014006356 C OMEPRAZOLE 1 ORAL
6810139 1014006357 C ALLOPURINOL 2 ORAL
6810139 1014006358 C LOSARTAN POTASSIUM 1 ORAL
6810139 1014006359 C METOCLOPRAMIDE 1 ORAL
6810139 1014006360 C TRAMADOL 2 ORAL
6810139 1014006361 C MICOSTATIN 2 UNKNOWN
6810139 1014006362 C PALMIDRONATE 2 PARENTERAL
6810139 1014006363 C LOVENOX 1 PARENTERAL
6810139 1014006364 C MORFEX 2 UNKNOWN
6810139 1014006365 C LEPONEX 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
6810139 1014006354 MULTIPLE MYELOMA
6810139 1014006355 MULTIPLE MYELOMA
6810139 1014006356 PROPHYLAXIS
6810139 1014006358 HYPERTENSION
6810139 1014006359 NAUSEA
6810139 1014006360 PAIN
6810139 1014006362 DRUG USE FOR UNKNOWN INDICATION
6810139 1014006363 THROMBOSIS PROPHYLAXIS
6810139 1014006364 INSOMNIA
6810139 1014006365 INSOMNIA

Outcome of event

Event ID OUTC COD
6810139 DE
6810139 HO

Reactions reported

Event ID PT
6810139 DRUG TOXICITY
6810139 PNEUMONIA
6810139 PULMONARY EMBOLISM
6810139 PULMONARY HYPERTENSION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6810139 1014006354 20100531 20100617 17 DAY
6810139 1014006355 20100531 20100617 17 DAY
6810139 1014006356 20100422
6810139 1014006357 20100422
6810139 1014006359 20100531
6810139 1014006360 20100611
6810139 1014006361 20100531
6810139 1014006362 20100528
6810139 1014006363 20100531