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
112108594 11210859 4 F 201407 20160908 20150622 20160914 EXP PHHY2015CA070181 NOVARTIS 43.71 YR F Y 0.00000 20160914 CN COUNTRY NOT SPECIFIED 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
112108594 11210859 1 PS NEORAL CYCLOSPORINE 1 Oral 150 MG, BID N 50715 150 MG BID
112108594 11210859 2 SS NEORAL CYCLOSPORINE 1 Oral 200 MG, BID N 50715 200 MG BID
112108594 11210859 3 SS NEORAL CYCLOSPORINE 1 Oral 300 MG, QD N 50715 300 MG QD
112108594 11210859 4 SS NEORAL CYCLOSPORINE 1 Oral 200 MG, QD N 50715 200 MG QD
112108594 11210859 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous 450 MG, BIW 6357.9834 MG 0 450 MG QOW
112108594 11210859 6 C VENTOLINE ALBUTEROL 1 Unknown N 0
112108594 11210859 7 C ALVESCO CICLESONIDE 1 Unknown 1 DF(1 PUFF), BID U 0 1 DF BID
112108594 11210859 8 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 1 DF(1 PUFF), BID U 0 1 DF BID
112108594 11210859 9 C ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Unknown N 0
112108594 11210859 10 C CETRIZINE CETIRIZINE HYDROCHLORIDE 1 Unknown 1 DF, BID U 0 1 DF TABLET BID
112108594 11210859 11 C SINGULAIR MONTELUKAST SODIUM 1 Unknown UNK U 0
112108594 11210859 12 C REACTINE /CAN/ 2 Unknown 20 MG, BID U 0 20 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112108594 11210859 1 Psoriasis
112108594 11210859 2 Eczema
112108594 11210859 5 Asthma
112108594 11210859 6 Product used for unknown indication
112108594 11210859 7 Product used for unknown indication
112108594 11210859 8 Product used for unknown indication
112108594 11210859 9 Product used for unknown indication
112108594 11210859 10 Product used for unknown indication
112108594 11210859 11 Product used for unknown indication
112108594 11210859 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112108594 11210859 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112108594 11210859 Asthma
112108594 11210859 Blood immunoglobulin E increased
112108594 11210859 Bronchitis
112108594 11210859 Confusional state
112108594 11210859 Cough
112108594 11210859 Dermatitis atopic
112108594 11210859 Diarrhoea
112108594 11210859 Drug ineffective
112108594 11210859 Eczema
112108594 11210859 Erythema
112108594 11210859 Forced expiratory volume decreased
112108594 11210859 Injection site warmth
112108594 11210859 Malaise
112108594 11210859 Neutrophil count increased
112108594 11210859 Overdose
112108594 11210859 Platelet count increased
112108594 11210859 Pruritus
112108594 11210859 Rales
112108594 11210859 Respiratory disorder
112108594 11210859 Sinusitis
112108594 11210859 Skin disorder
112108594 11210859 Stress
112108594 11210859 Vomiting
112108594 11210859 Wheezing
112108594 11210859 White blood cell count increased

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
112108594 11210859 1 2014 0
112108594 11210859 2 2014 0
112108594 11210859 3 2014 0
112108594 11210859 4 2014 0
112108594 11210859 5 20150716 20160706 0