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
127377671 12737767 1 I 20160909 0 20160912 20160912 DIR US-FDA-350361 FDA-CTU 8.00 YR M N 23.85000 KG 20160912 N 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
127377671 12737767 1 PS SINGULAIR MONTELUKAST SODIUM 1 Oral 0
127377671 12737767 3 C FLOVENT FLUTICASONE PROPIONATE 1 0
127377671 12737767 5 C SINGULAIR MONTELUKAST SODIUM 1 0
127377671 12737767 7 C OTC UNSPECIFIED INGREDIENT 1 0
127377671 12737767 9 C PROAIR HFA ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127377671 12737767 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
127377671 12737767 OT
127377671 12737767 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127377671 12737767 Abnormal behaviour
127377671 12737767 Anxiety
127377671 12737767 Disturbance in attention
127377671 12737767 Fear
127377671 12737767 Fear of death
127377671 12737767 Learning disorder
127377671 12737767 Memory impairment
127377671 12737767 Nervousness
127377671 12737767 Nightmare

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
127377671 12737767 1 20131023 20160908 0