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
110540753 11054075 3 F 20160623 20150422 20160706 EXP CA-ROCHE-1426946 ROCHE 0.00 F Y 0.00000 20160706 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
110540753 11054075 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 150 MG
110540753 11054075 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976
110540753 11054075 3 C DEXILANT DEXLANSOPRAZOLE 1 0
110540753 11054075 4 C SINGULAIR MONTELUKAST SODIUM 1 0
110540753 11054075 5 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
110540753 11054075 6 C AVAMYS FLUTICASONE FUROATE 1 0
110540753 11054075 7 C VENTOLINE ALBUTEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110540753 11054075 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
110540753 11054075 HO
110540753 11054075 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110540753 11054075 Asthenia
110540753 11054075 Hypercalcaemia
110540753 11054075 Hyperthyroidism
110540753 11054075 Hypocalcaemia
110540753 11054075 Hypoglycaemia
110540753 11054075 Insomnia
110540753 11054075 Malaise
110540753 11054075 Nasopharyngitis
110540753 11054075 Papillary thyroid cancer
110540753 11054075 Presyncope
110540753 11054075 Weight decreased

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
110540753 11054075 1 20060908 0
110540753 11054075 2 20150402 0