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
103980377 10398037 7 F 20131229 20160720 20140821 20160727 EXP CA-ROCHE-1452780 ROCHE 65.76 YR F Y 0.00000 20160727 CN CA 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
103980377 10398037 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0051B/S0053A,S00002F 103976 300 MG SOLUTION FOR INJECTION QOW
103980377 10398037 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0051B/S0053A,S00002F 103976 SOLUTION FOR INJECTION
103980377 10398037 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0051B/S0053A,S00002F 103976 SOLUTION FOR INJECTION
103980377 10398037 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0051B/S0053A,S00002F 103976 SOLUTION FOR INJECTION
103980377 10398037 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0051B/S0053A,S00002F 103976 SOLUTION FOR INJECTION
103980377 10398037 6 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0051B/S0053A,S00002F 103976 SOLUTION FOR INJECTION
103980377 10398037 7 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Unknown U 0
103980377 10398037 8 C VENTOLIN ALBUTEROL SULFATE 1 Unknown U 0
103980377 10398037 9 C SINGULAIR MONTELUKAST SODIUM 1 Unknown U 0
103980377 10398037 10 C AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Unknown U 0
103980377 10398037 11 C FOSAMAX ALENDRONATE SODIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103980377 10398037 1 Asthma
103980377 10398037 7 Product used for unknown indication
103980377 10398037 8 Product used for unknown indication
103980377 10398037 9 Product used for unknown indication
103980377 10398037 10 Product used for unknown indication
103980377 10398037 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
103980377 10398037 OT
103980377 10398037 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
103980377 10398037 Asthma
103980377 10398037 Blood pressure increased
103980377 10398037 Bronchitis
103980377 10398037 Cough
103980377 10398037 Diabetes mellitus
103980377 10398037 Dizziness
103980377 10398037 Headache
103980377 10398037 Influenza
103980377 10398037 Oropharyngeal pain
103980377 10398037 Pneumonia

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
103980377 10398037 1 20130319 0
103980377 10398037 2 201312 201312 0
103980377 10398037 4 20160429 0
103980377 10398037 5 20160527 0
103980377 10398037 6 20160623 0