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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127601151 | 12760115 | 1 | I | 201504 | 20160906 | 20160919 | 20160919 | EXP | CA-VALIDUS PHARMACEUTICALS LLC-CA-2016VAL002639 | VALIDUS | 0.00 | Y | 0.00000 | 20160919 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127601151 | 12760115 | 1 | PS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | 25 MG, BID | U | 17963 | 25 | MG | |||||||
127601151 | 12760115 | 2 | SS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | UNK | U | 17963 | |||||||||
127601151 | 12760115 | 3 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | 300 MG, BIW | Y | 0 | 300 | MG | |||||||
127601151 | 12760115 | 4 | SS | SEEBRI BREEZHALER | GLYCOPYRROLATE | 1 | 1 DF(1 PUFF), QD | Y | 0 | 1 | DF | INHALATION POWDER | |||||||
127601151 | 12760115 | 5 | C | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK | U | 0 | ||||||||||
127601151 | 12760115 | 6 | C | OXEZE | 2 | UNK | U | 0 | |||||||||||
127601151 | 12760115 | 7 | C | PREDNISONE. | PREDNISONE | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127601151 | 12760115 | 1 | Heart rate irregular |
127601151 | 12760115 | 3 | Asthma |
127601151 | 12760115 | 4 | Asthma |
127601151 | 12760115 | 5 | Product used for unknown indication |
127601151 | 12760115 | 6 | Product used for unknown indication |
127601151 | 12760115 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127601151 | 12760115 | HO |
127601151 | 12760115 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127601151 | 12760115 | Appendicitis | |
127601151 | 12760115 | Body temperature increased | |
127601151 | 12760115 | Feeling abnormal | |
127601151 | 12760115 | Heart rate irregular | |
127601151 | 12760115 | Myocardial infarction | |
127601151 | 12760115 | Obstructive airways disorder | |
127601151 | 12760115 | Pericarditis | |
127601151 | 12760115 | Product use issue |
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 |
---|---|---|---|---|---|---|
127601151 | 12760115 | 1 | 201501 | 0 | ||
127601151 | 12760115 | 2 | 201509 | 0 | ||
127601151 | 12760115 | 3 | 20150218 | 20150326 | 0 | |
127601151 | 12760115 | 4 | 20151210 | 20160825 | 0 |