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
110147013 11014701 3 F 201310 20160720 20150412 20160728 EXP US-JNJFOC-20140903678 JANSSEN 62.09 YR A F Y 104.33000 KG 20160728 CN 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
110147013 11014701 1 SS ULTRAM TRAMADOL HYDROCHLORIDE 1 Oral EVERY 6-8 HOURS U UNKNOWN 0 50 MG TABLETS Q6H
110147013 11014701 2 PS ULTRAM TRAMADOL HYDROCHLORIDE 1 Oral EVERY 6-8 HOURS U UNKNOWN 20281 50 MG TABLETS Q6H
110147013 11014701 3 C HYZAAR HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM 1 Unknown 0 UNSPECIFIED
110147013 11014701 4 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 0 400 MG TABLET QD
110147013 11014701 5 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 0 150 MG TABLET QD
110147013 11014701 6 C HYDROCODONE HYDROCODONE 1 Oral 1-2 TABLETS, AS NEEDED 0 325 MG TABLET
110147013 11014701 7 C CHOLESTYRAMINE. CHOLESTYRAMINE 1 Oral 1 PACKET TWICE DAILY 0
110147013 11014701 8 C LOSARTAN. LOSARTAN 1 Unknown 0 12.5 MG UNSPECIFIED QD
110147013 11014701 9 C ZYPREXA OLANZAPINE 1 Unknown 0 7.5 MG UNSPECIFIED QD
110147013 11014701 10 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 Oral 0 20 MEQ UNSPECIFIED BID
110147013 11014701 11 C LYRICA PREGABALIN 1 Unknown 0 150 MG UNSPECIFIED BID
110147013 11014701 12 C REVATIO SILDENAFIL CITRATE 1 Unknown 0 20 MG UNSPECIFIED TID
110147013 11014701 13 C LIORESAL BACLOFEN 1 Unknown 0 10 MG UNSPECIFIED TID
110147013 11014701 14 C ATENOLOL. ATENOLOL 1 Unknown 0 100 MG UNSPECIFIED QD
110147013 11014701 15 C CLONOPIN CLONAZEPAM 1 Unknown 0 1 MG UNSPECIFIED TID
110147013 11014701 16 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110147013 11014701 1 Headache
110147013 11014701 2 Pain
110147013 11014701 3 Product used for unknown indication
110147013 11014701 4 Depression
110147013 11014701 5 Depression
110147013 11014701 6 Pain
110147013 11014701 7 Gastric disorder
110147013 11014701 8 Blood pressure measurement
110147013 11014701 9 Depression
110147013 11014701 10 Depression
110147013 11014701 11 Depression
110147013 11014701 12 Pulmonary arterial hypertension
110147013 11014701 13 Muscle relaxant therapy
110147013 11014701 14 Blood pressure measurement
110147013 11014701 15 Anxiety
110147013 11014701 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
110147013 11014701 HO
110147013 11014701 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110147013 11014701 Adverse drug reaction
110147013 11014701 Hypersensitivity
110147013 11014701 Hypopnoea
110147013 11014701 Seizure

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
110147013 11014701 1 201310 20131016 0
110147013 11014701 2 201310 20131016 0