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 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
123685196 12368519 6 F 2016 20160718 20160513 20160802 EXP CA-VALIDUS PHARMACEUTICALS LLC-CA-2016VAL001536 VALIDUS 0.00 Y 0.00000 20160802 CN CA CA

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
123685196 12368519 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Unknown UNK U 17963
123685196 12368519 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, QMO (ONCE A MONTH) Y 0 40 MG
123685196 12368519 3 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous UNK, SINGLE/ONCE Y 0
123685196 12368519 4 SS PAMIDRONATE PAMIDRONATE DISODIUM 1 Intravenous (not otherwise specified) UNK U 0
123685196 12368519 5 C LANTUS INSULIN GLARGINE 1 UNK U 0
123685196 12368519 6 C EZETROL EZETIMIBE 1 UNK U 0
123685196 12368519 7 C LIPITOR ATORVASTATIN CALCIUM 1 UNK U 0
123685196 12368519 8 C METFORMIN METFORMIN HYDROCHLORIDE 1 UNK U 0
123685196 12368519 9 C BABY ASPIRIN ASPIRIN 1 UNK U 0
123685196 12368519 10 C COZAAR LOSARTAN POTASSIUM 1 UNK U 0
123685196 12368519 11 C LASIX FUROSEMIDE 1 UNK U 0
123685196 12368519 12 C PLAVIX CLOPIDOGREL BISULFATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123685196 12368519 1 Product used for unknown indication
123685196 12368519 2 Acromegaly
123685196 12368519 3 Acromegaly
123685196 12368519 4 Blood calcium increased
123685196 12368519 5 Product used for unknown indication
123685196 12368519 6 Product used for unknown indication
123685196 12368519 7 Product used for unknown indication
123685196 12368519 8 Product used for unknown indication
123685196 12368519 9 Product used for unknown indication
123685196 12368519 10 Product used for unknown indication
123685196 12368519 11 Product used for unknown indication
123685196 12368519 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123685196 12368519 HO
123685196 12368519 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123685196 12368519 Blood pressure increased
123685196 12368519 Chills
123685196 12368519 Dyspnoea
123685196 12368519 Dyspnoea exertional
123685196 12368519 Feeling abnormal
123685196 12368519 Injection site pain
123685196 12368519 Injection site swelling
123685196 12368519 Night sweats
123685196 12368519 Platelet count decreased
123685196 12368519 Pulmonary embolism
123685196 12368519 Pyrexia
123685196 12368519 Sepsis
123685196 12368519 Thrombosis
123685196 12368519 Tremor

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
123685196 12368519 2 20111217 20160718 0
123685196 12368519 3 20110902 20110902 0
123685196 12368519 4 20160322 0