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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127340061 | 12734006 | 1 | I | 20120426 | 20160912 | 20160912 | PER | US-ASTRAZENECA-2012SE27362 | ASTRAZENECA | 58.00 | YR | M | Y | 90.70000 | KG | 20160913 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127340061 | 12734006 | 1 | PS | PULMICORT RESPULES | BUDESONIDE | 1 | Respiratory (inhalation) | U | U | 20929 | .5 | MG | NEBULISER SUSPENSION | BID | |||||
| 127340061 | 12734006 | 2 | SS | PULMICORT RESPULES | BUDESONIDE | 1 | Respiratory (inhalation) | U | U | 20929 | .5 | MG | NEBULISER SUSPENSION | BID | |||||
| 127340061 | 12734006 | 3 | SS | PULMICORT RESPULES | BUDESONIDE | 1 | Respiratory (inhalation) | U | U | 20929 | .5 | MG | NEBULISER SUSPENSION | BID | |||||
| 127340061 | 12734006 | 4 | SS | PULMICORT RESPULES | BUDESONIDE | 1 | Respiratory (inhalation) | 0.25 MG DAILY TO BE MIXED WITH 1/8 TO 1/4 TEASPOONFUL OF SALT IN 8 OUNCE OF WATER | U | U | 20929 | NEBULISER SUSPENSION | |||||||
| 127340061 | 12734006 | 5 | SS | PULMICORT RESPULES | BUDESONIDE | 1 | Respiratory (inhalation) | 0.25 MG DAILY TO BE MIXED WITH 1/8 TO 1/4 TEASPOONFUL OF SALT IN 8 OUNCE OF WATER | U | U | 20929 | NEBULISER SUSPENSION | |||||||
| 127340061 | 12734006 | 6 | SS | PULMICORT RESPULES | BUDESONIDE | 1 | Respiratory (inhalation) | 0.25 MG DAILY TO BE MIXED WITH 1/8 TO 1/4 TEASPOONFUL OF SALT IN 8 OUNCE OF WATER | U | U | 20929 | NEBULISER SUSPENSION | |||||||
| 127340061 | 12734006 | 7 | SS | RHINOCORT AQUA | BUDESONIDE | 1 | Nasal | N | U | 20746 | NASAL SPRAY | ||||||||
| 127340061 | 12734006 | 8 | C | MULTIVITAMIN | VITAMINS | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127340061 | 12734006 | 1 | Sinusitis |
| 127340061 | 12734006 | 2 | Rhinitis allergic |
| 127340061 | 12734006 | 3 | Multiple allergies |
| 127340061 | 12734006 | 4 | Sinusitis |
| 127340061 | 12734006 | 5 | Rhinitis allergic |
| 127340061 | 12734006 | 6 | Multiple allergies |
| 127340061 | 12734006 | 7 | Multiple allergies |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127340061 | 12734006 | Circumstance or information capable of leading to medication error | |
| 127340061 | 12734006 | Drug administered to patient of inappropriate age | |
| 127340061 | 12734006 | Drug effect incomplete | |
| 127340061 | 12734006 | Intentional product misuse | |
| 127340061 | 12734006 | Intercepted drug prescribing error | |
| 127340061 | 12734006 | Off label use | |
| 127340061 | 12734006 | Product use issue | |
| 127340061 | 12734006 | Upper respiratory tract infection |
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 |
|---|---|---|---|---|---|---|
| 127340061 | 12734006 | 4 | 20120604 | 0 | ||
| 127340061 | 12734006 | 5 | 20120604 | 0 | ||
| 127340061 | 12734006 | 6 | 20120604 | 0 |