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
126967501 12696750 1 I 20160616 20160830 20160830 PER PT-LUPIN PHARMACEUTICALS INC.-2016-02846 LUPIN ALMEIDA J, LOPES A, BARBOSA M. HYPERSENSITIVITY TO PROTON PUMP INHIBITORS. REVISTA PORTUGUESADE IMUNOALERGOLOGIA. 2016;24(1):31-36. 39.00 YR F Y 0.00000 20160825 OT PT PT

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
126967501 12696750 1 SS IBUPROFEN. IBUPROFEN 1 Oral UNKNOWN 0 400 MG
126967501 12696750 2 SS ASPIRIN. ASPIRIN 1 Intravenous (not otherwise specified) UNKNOWN 0
126967501 12696750 3 PS OMEPRAZOLE. OMEPRAZOLE 1 Intravenous (not otherwise specified) UNKNOWN 202384
126967501 12696750 4 SS OMEPRAZOLE. OMEPRAZOLE 1 UNKNOWN 202384 20 MG
126967501 12696750 5 SS OMEPRAZOLE. OMEPRAZOLE 1 40 MG UNKNOWN 202384
126967501 12696750 6 SS LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown UNKNOWN 0
126967501 12696750 7 SS Pantoprazole PANTOPRAZOLE SODIUM 1 Unknown UNKNOWN 0
126967501 12696750 8 SS Esomeprazole ESOMEPRAZOLE 1 Unknown UNKNOWN 0
126967501 12696750 9 SS Rabeprazole RABEPRAZOLE 1 Unknown UNKNOWN 78964

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126967501 12696750 1 Product used for unknown indication
126967501 12696750 2 Influenza like illness
126967501 12696750 3 Gastrooesophageal reflux disease
126967501 12696750 6 Gastrooesophageal reflux disease
126967501 12696750 7 Gastrooesophageal reflux disease
126967501 12696750 8 Gastrooesophageal reflux disease
126967501 12696750 9 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
126967501 12696750 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126967501 12696750 Angioedema
126967501 12696750 Dermatitis bullous
126967501 12696750 Rash generalised

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
126967501 12696750 2 2007 0
126967501 12696750 3 2007 0
126967501 12696750 5 2010 0