The Safety Rates Drug Report

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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
118540893 11854089 3 F 2015 20160113 20151219 20160128 EXP JP-UCBSA-2015040247 UCB 73.00 YR M Y 0.00000 20160125 MD JP JP

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
118540893 11854089 1 PS XYZAL LEVOCETIRIZINE DIHYDROCHLORIDE 1 Oral 5 MG, ONCE DAILY (QD) 325 MG 22064 5 MG FILM-COATED TABLET QD
118540893 11854089 2 SS XYZAL LEVOCETIRIZINE DIHYDROCHLORIDE 1 325 MG 22064 FILM-COATED TABLET
118540893 11854089 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 120 MG, ONCE DAILY (QD) 8640 MG U 0 120 MG QD
118540893 11854089 4 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 8640 MG U 0
118540893 11854089 5 SS POLARAMINE DEXCHLORPHENIRAMINE MALEATE 1 Oral 4 MG, ONCE DAILY (QD) 76 MG U 0 4 MG QD
118540893 11854089 6 SS POLARAMINE DEXCHLORPHENIRAMINE MALEATE 1 76 MG U 0
118540893 11854089 7 C Atorvastatin ATORVASTATIN 1 UNK U 0
118540893 11854089 8 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK U 0
118540893 11854089 9 C Omepral OMEPRAZOLE 1 UNK U 0
118540893 11854089 10 C VESICARE SOLIFENACIN SUCCINATE 1 UNK U 0
118540893 11854089 11 C Carbocisteine CARBOCYSTEINE 1 UNK U 0
118540893 11854089 12 C Geninax GARENOXACIN MESYLATE 1 UNK U 0
118540893 11854089 13 C Mucodyne CARBOCYSTEINE 1 UNK U 0
118540893 11854089 14 C ASVERIN (TIPEPIDINE HIBENZATE) TIPEPIDINE HIBENZATE 1 UNK U 0
118540893 11854089 15 C PL ACETAMINOPHENCAFFEINEPROMETHAZINESALICYLAMIDE 1 UNK U 0
118540893 11854089 16 C AVAPRO IRBESARTAN 1 UNK U 0
118540893 11854089 17 C CELESTAMINE BETAMETHASONEDEXCHLORPHENIRAMINE MALEATE 1 3 DF, UNK U 0 3 DF
118540893 11854089 18 C CELESTAMINE BETAMETHASONEDEXCHLORPHENIRAMINE MALEATE 1 2 DF, UNK U 0 2 DF
118540893 11854089 19 C CELESTAMINE BETAMETHASONEDEXCHLORPHENIRAMINE MALEATE 1 1 DF, UNK U 0 1 DF
118540893 11854089 20 C Sulbacillin AMPICILLIN SODIUMSULBACTAM SODIUM 1 Intravenous (not otherwise specified) UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118540893 11854089 1 Pruritus
118540893 11854089 2 Rash generalised
118540893 11854089 3 Pruritus
118540893 11854089 4 Rash generalised
118540893 11854089 5 Pruritus
118540893 11854089 6 Rash generalised
118540893 11854089 7 Product used for unknown indication
118540893 11854089 8 Product used for unknown indication
118540893 11854089 9 Product used for unknown indication
118540893 11854089 10 Product used for unknown indication
118540893 11854089 11 Product used for unknown indication
118540893 11854089 12 Product used for unknown indication
118540893 11854089 13 Product used for unknown indication
118540893 11854089 14 Product used for unknown indication
118540893 11854089 15 Product used for unknown indication
118540893 11854089 16 Product used for unknown indication
118540893 11854089 17 Rash
118540893 11854089 20 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118540893 11854089 HO
118540893 11854089 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118540893 11854089 Disseminated intravascular coagulation
118540893 11854089 Eosinophil count increased
118540893 11854089 Platelet count decreased
118540893 11854089 Pneumonia
118540893 11854089 Pyrexia
118540893 11854089 Rash

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
118540893 11854089 1 20150525 20151105 0
118540893 11854089 3 20150518 20151105 0
118540893 11854089 5 20150710 20151105 0
118540893 11854089 17 20150803 2015 0
118540893 11854089 18 2015 2015 0
118540893 11854089 19 20151006 0
118540893 11854089 20 2015 0