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
127577601 12757760 1 I 20100507 20100528 20160919 20160919 EXP AU-009507513-1006USA00105 MERCK 36.00 MON M Y 0.00000 20160919 OT AU AU

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
127577601 12757760 1 PS SINGULAIR MONTELUKAST SODIUM 1 Oral 4 MG, QD 60 MG 20830 4 MG CHEWABLE TABLET QD
127577601 12757760 2 SS SINGULAIR MONTELUKAST SODIUM 1 60 MG 20830 CHEWABLE TABLET
127577601 12757760 3 SS SINGULAIR MONTELUKAST SODIUM 1 60 MG 20830 CHEWABLE TABLET
127577601 12757760 4 C FLIXOTIDE FLUTICASONE PROPIONATE 1 0
127577601 12757760 5 C NASONEX MOMETASONE FUROATE 1 0 NASAL DROPS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127577601 12757760 1 Rhinitis allergic
127577601 12757760 2 Asthma
127577601 12757760 3 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127577601 12757760 Abdominal pain upper
127577601 12757760 Abnormal behaviour
127577601 12757760 Aggression
127577601 12757760 Frustration tolerance decreased
127577601 12757760 Physical assault

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
127577601 12757760 1 20100423 20100527 0