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
126186962 12618696 2 F 20160915 20160803 20160923 EXP US-AMGEN-USASP2016098175 AMGEN 44.00 YR A F Y 69.40000 KG 20160923 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
126186962 12618696 1 PS ARANESP DARBEPOETIN ALFA 1 Subcutaneous UNK U 103951 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
126186962 12618696 2 C PROCRIT ERYTHROPOIETIN 1 Unknown 20.000 UNIT, QWK U 0 SOLUTION FOR INJECTION /wk
126186962 12618696 3 C PULMICORT TURBUHALER BUDESONIDE 1 0.5 MG/2 ML, UNK 0 .5 MG
126186962 12618696 4 C KLONOPIN CLONAZEPAM 1 0.5 MG, UNK 0 .5 MG
126186962 12618696 5 C CATAPRES CLONIDINE HYDROCHLORIDE 1 0.3 MG, UNK 0 .3 MG
126186962 12618696 6 C CARDURA DOXAZOSIN MESYLATE 1 8 MG, UNK 0 8 MG
126186962 12618696 7 C FERROUS SULFATE. FERROUS SULFATE 1 325 MG, UNK 0 325 MG
126186962 12618696 8 C FLONASE FLUTICASONE PROPIONATE 1 50 MUG, UNK 0 50 UG
126186962 12618696 9 C NEPHRO VITE RX ASCORBIC ACIDBIOTINCALCIUM PANTOTHENATECYANOCOBALAMINFOLIC ACIDNIACINAMIDEPYRIDOXINE HYDROCHLORIDERIBOFLAVINTHIAMINE MONONITRATE 1 0.8 MG, UNK 0 .8 MG
126186962 12618696 10 C APRESOLINE HYDROCHLORIDE HYDRALAZINE HYDROCHLORIDE 1 100 MG, UNK 0 100 MG
126186962 12618696 11 C LOPRESSOR METOPROLOL TARTRATE 1 100 MG, UNK 0 100 MG
126186962 12618696 12 C DULERA FORMOTEROL FUMARATE DIHYDRATEMOMETASONE FUROATE 1 100-5 MCG 0
126186962 12618696 13 C SINGULAIR MONTELUKAST SODIUM 1 10 MG, UNK 0 10 MG
126186962 12618696 14 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 500 MG, UNK 0 500 MG
126186962 12618696 15 C DELTASONE PREDNISONE 1 5 MG, UNK 0 5 MG
126186962 12618696 16 C SODIUM BICARBONATE. SODIUM BICARBONATE 1 648 MG, UNK 0 648 MG
126186962 12618696 17 C KAYEXALATE SODIUM POLYSTYRENE SULFONATE 1 15 G/60 ML, UNK 0 15 G
126186962 12618696 18 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 0.5 MG, UNK 0 .5 MG
126186962 12618696 19 C ROCALTROL CALCITRIOL 1 0.25 MUG, UNK 0 .25 UG
126186962 12618696 20 C LASIX FUROSEMIDE 1 40 MG, UNK 0 40 MG
126186962 12618696 21 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 325 MG, UNK 0 325 MG
126186962 12618696 22 C FLORANEX LACTOBACILLUS ACIDOPHILUSLACTOBACILLUS DELBRUECKII SUBSP. BULGARICUS 1 1 MILLION CELL 0
126186962 12618696 23 C PRINIVIL LISINOPRIL 1 20 MG, UNK 0 20 MG
126186962 12618696 24 C ZESTRIL LISINOPRIL 1 20 MG, UNK 0 20 MG
126186962 12618696 25 C CARDENE NICARDIPINE HYDROCHLORIDE 1 30 MG, UNK 0 30 MG
126186962 12618696 26 C PROTONIX PANTOPRAZOLE SODIUM 1 40 MG, UNK 0 40 MG
126186962 12618696 27 C CARAFATE SUCRALFATE 1 1 G, UNK 0 1 G
126186962 12618696 28 C AMBIEN ZOLPIDEM TARTRATE 1 10 MG, UNK 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126186962 12618696 1 Anaemia
126186962 12618696 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126186962 12618696 HO
126186962 12618696 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126186962 12618696 Abdominal pain
126186962 12618696 Anxiety
126186962 12618696 Clostridium difficile colitis
126186962 12618696 Constipation
126186962 12618696 Cough
126186962 12618696 Drug effect decreased
126186962 12618696 Dyspnoea
126186962 12618696 Feeling abnormal
126186962 12618696 Haemoglobin abnormal
126186962 12618696 Headache
126186962 12618696 Hyperkalaemia
126186962 12618696 Hypertension
126186962 12618696 Hypertensive crisis
126186962 12618696 Hypotension
126186962 12618696 Metabolic acidosis
126186962 12618696 Pancreatitis
126186962 12618696 Pneumonia
126186962 12618696 Pneumonia pseudomonal
126186962 12618696 Pyrexia
126186962 12618696 Tachycardia
126186962 12618696 Tracheobronchitis

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
126186962 12618696 2 201602 0