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
126718501 12671850 1 I 200704 20070202 20160822 20160822 EXP US-ROCHE-GNE237449 ROCHE 20.59 YR F Y 0.00000 20160822 CN US US

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
126718501 12671850 1 PS Omalizumab OMALIZUMAB 1 Subcutaneous UNK UNK, UNKNOWN U NOT REPORTED 5369 SOLUTION FOR INJECTION
126718501 12671850 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
126718501 12671850 3 C ALBUTEROL. ALBUTEROL 1 0
126718501 12671850 4 C CLARINEX DESLORATADINE 1 0
126718501 12671850 5 C SINGULAIR MONTELUKAST SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126718501 12671850 1 Asthma
126718501 12671850 2 Asthma
126718501 12671850 3 Asthma
126718501 12671850 4 Hypersensitivity
126718501 12671850 5 Asthma

Outcome of event

Event ID CASEID OUTC COD
126718501 12671850 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126718501 12671850 Asthma
126718501 12671850 Exposure during pregnancy
126718501 12671850 Gastroenteritis viral
126718501 12671850 Urinary tract infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found