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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98898023 | 9889802 | 3 | F | 20130729 | 20140211 | 20140212 | 20151001 | EXP | US-ROCHE-1323434 | ROCHE | 52.60 | YR | M | Y | 90.80000 | KG | 20151001 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98898023 | 9889802 | 1 | PS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | 103976 | 150 | MG | SOLUTION FOR INJECTION | /month | |||||||
| 98898023 | 9889802 | 2 | C | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | 0 | 115 | MG | QD | ||||||||
| 98898023 | 9889802 | 3 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | Oral | 0 | 10 | MG | QD | ||||||||
| 98898023 | 9889802 | 4 | C | ACIPHEX | RABEPRAZOLE SODIUM | 1 | Oral | 0 | 20 | MG | QD | ||||||||
| 98898023 | 9889802 | 5 | C | ACIPHEX | RABEPRAZOLE SODIUM | 1 | 0 | ||||||||||||
| 98898023 | 9889802 | 6 | C | PULMICORT TURBUHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 0 | |||||||||||
| 98898023 | 9889802 | 7 | C | GENTAMICIN. | GENTAMICIN | 1 | Respiratory (inhalation) | FOR 5 YEARS, REMOVED FROM THE RINSE 3 MONTHS AGO | 0 | BID | |||||||||
| 98898023 | 9889802 | 8 | C | BUDESONIDE. | BUDESONIDE | 1 | Oral | START 5 YEARS AGO | 0 | BID | |||||||||
| 98898023 | 9889802 | 9 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 0 | 15 | MG | |||||||||
| 98898023 | 9889802 | 10 | C | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Unknown | HFA 230 2 PUFF BID | 0 | ||||||||||
| 98898023 | 9889802 | 11 | C | XYZAL | LEVOCETIRIZINE DIHYDROCHLORIDE | 1 | 0 | ||||||||||||
| 98898023 | 9889802 | 12 | C | LEXAPRO | ESCITALOPRAM OXALATE | 1 | 0 | ||||||||||||
| 98898023 | 9889802 | 13 | C | BROVANA | ARFORMOTEROL TARTRATE | 1 | 0 | ||||||||||||
| 98898023 | 9889802 | 14 | C | PULMICORT TURBUHALER | BUDESONIDE | 1 | 0 | ||||||||||||
| 98898023 | 9889802 | 15 | C | PROVENTIL HFA | ALBUTEROL SULFATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 98898023 | 9889802 | 1 | Asthma |
| 98898023 | 9889802 | 2 | Asthma |
| 98898023 | 9889802 | 3 | Asthma |
| 98898023 | 9889802 | 4 | Asthma |
| 98898023 | 9889802 | 5 | Gastrooesophageal reflux disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 98898023 | 9889802 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 98898023 | 9889802 | Alopecia | |
| 98898023 | 9889802 | Amnesia | |
| 98898023 | 9889802 | Paraesthesia | |
| 98898023 | 9889802 | Sensory disturbance | |
| 98898023 | 9889802 | Vertigo |
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 |
|---|---|---|---|---|---|---|
| 98898023 | 9889802 | 1 | 2009 | 0 | ||
| 98898023 | 9889802 | 7 | 2013 | 0 |