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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123698042 | 12369804 | 2 | F | 201604 | 20160512 | 20160516 | 20160724 | PER | US-ASTRAZENECA-2016SE43046 | ASTRAZENECA | 856.00 | MON | F | Y | 47.60000 | KG | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123698042 | 12369804 | 1 | PS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 MICROGRAMS, ONE PUFF TWICE DAILY. | BACK | 21949 | INHALATION POWDER | ||||||||
| 123698042 | 12369804 | 2 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 MICROGRAMS, ONE PUFF TWO TIMES A DAY | BACK | 21949 | INHALATION POWDER | ||||||||
| 123698042 | 12369804 | 3 | SS | PULMICORT FLEXHALER | BUDESONIDE | 1 | Respiratory (inhalation) | 90 MICROGRAMS, ONE PUFF TWO TIMES A DAY | BACK | 21949 | INHALATION POWDER | ||||||||
| 123698042 | 12369804 | 4 | C | RECLAST | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | YEARLY | 0 | ||||||||||
| 123698042 | 12369804 | 5 | C | A DIURETIC | 2 | Oral | DAILY | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123698042 | 12369804 | 1 | Asthma |
| 123698042 | 12369804 | 2 | Asthma |
| 123698042 | 12369804 | 3 | Asthma |
| 123698042 | 12369804 | 4 | Osteoporosis |
| 123698042 | 12369804 | 5 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123698042 | 12369804 | Circumstance or information capable of leading to medication error | |
| 123698042 | 12369804 | Oral discomfort | |
| 123698042 | 12369804 | Osteoporosis | |
| 123698042 | 12369804 | Product quality issue | |
| 123698042 | 12369804 | Stomatitis |
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 |
|---|---|---|---|---|---|---|
| 123698042 | 12369804 | 5 | 2014 | 0 |