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
114923947 11492394 7 F 20140925 20160923 20150910 20160928 EXP PHHY2014CA128928 NOVARTIS 53.85 YR F Y 0.00000 20160928 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
114923947 11492394 1 SS XOLAIR OMALIZUMAB 1 Subcutaneous 375 MG, BIW U 0 375 MG QOW
114923947 11492394 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U 0
114923947 11492394 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U 0
114923947 11492394 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U 0
114923947 11492394 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U 0
114923947 11492394 6 PS DIOVAN VALSARTAN 1 Oral U 20665
114923947 11492394 7 C ALVESCO CICLESONIDE 1 Unknown U 0
114923947 11492394 8 C VENTOLIN ALBUTEROL SULFATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114923947 11492394 1 Asthma
114923947 11492394 6 Product used for unknown indication
114923947 11492394 7 Product used for unknown indication
114923947 11492394 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114923947 11492394 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114923947 11492394 Blood pressure systolic increased
114923947 11492394 Bronchitis
114923947 11492394 Cough
114923947 11492394 Diarrhoea
114923947 11492394 Dizziness
114923947 11492394 Drug hypersensitivity
114923947 11492394 Fatigue
114923947 11492394 Gastrointestinal disorder
114923947 11492394 Headache
114923947 11492394 Influenza
114923947 11492394 Injection site hyperaesthesia
114923947 11492394 Injection site hypersensitivity
114923947 11492394 Injection site hypoaesthesia
114923947 11492394 Injection site pain
114923947 11492394 Malaise
114923947 11492394 Nausea
114923947 11492394 Oropharyngeal pain
114923947 11492394 Pain
114923947 11492394 Pyrexia

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
114923947 11492394 1 20140911 0
114923947 11492394 2 20140925 0
114923947 11492394 3 20151105 0
114923947 11492394 4 20151217 0
114923947 11492394 5 20160825 0