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 |