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
127409341 12740934 1 I 20160909 20160914 20160914 EXP CA-009507513-1609CAN005055 MERCK 11.00 YR M Y 46.00000 KG 20160914 OT 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
127409341 12740934 1 PS GRASTEK PHLEUM PRATENSE POLLEN 1 Oral U 125473 SUBLINGUAL TABLET
127409341 12740934 2 SS SINGULAIR MONTELUKAST SODIUM 1 Unknown 5.0 MILLIGRAM, 1 EVERY 1 DAY U 0 5 MG TABLET QD
127409341 12740934 3 C ALVESCO CICLESONIDE 1 0
127409341 12740934 4 C VENTOLIN ALBUTEROL SULFATE 1 0
127409341 12740934 5 C VENTOLIN HFA ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127409341 12740934 1 Seasonal allergy
127409341 12740934 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
127409341 12740934 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127409341 12740934 Abdominal pain upper
127409341 12740934 Dyspnoea
127409341 12740934 Pharyngeal paraesthesia

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

no results found

Therapies reported

no results found