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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124550922 | 12455092 | 2 | F | 20160523 | 20160701 | 20160610 | 20160712 | EXP | US-JNJFOC-20160526918 | JOHNSON AND JOHNSON | 83.69 | YR | E | F | Y | 54.43000 | KG | 20160712 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124550922 | 12455092 | 1 | PS | BENADRYL ALLERGY LIQUI-GELS | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | 1 GEL (UNIT UNSPECIFIED), ONCE | Y | N | UNKNOWN | 999999 | 25 | MG | CAPSULE | ||||
| 124550922 | 12455092 | 2 | SS | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 3 PILLS (UNSPECIFIEDS UNIT), 1 DAY | U | 0 | UNSPECIFIED | ||||||||
| 124550922 | 12455092 | 3 | SS | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | U | 0 | 500 | MG | UNSPECIFIED | |||||||
| 124550922 | 12455092 | 4 | SS | SEPTOCAINE | ARTICAINE HYDROCHLORIDEEPINEPHRINE BITARTRATE | 1 | Unknown | U | 0 | UNSPECIFIED | |||||||||
| 124550922 | 12455092 | 5 | SS | ALL OTHER THERAPEUTIC PRODUCTS | UNSPECIFIED INGREDIENT | 1 | Unknown | U | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124550922 | 12455092 | 1 | Nasal pruritus |
| 124550922 | 12455092 | 2 | Tooth extraction |
| 124550922 | 12455092 | 3 | Tooth extraction |
| 124550922 | 12455092 | 4 | Product used for unknown indication |
| 124550922 | 12455092 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124550922 | 12455092 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124550922 | 12455092 | Aphonia | |
| 124550922 | 12455092 | Dyspnoea | |
| 124550922 | 12455092 | Expired product administered | |
| 124550922 | 12455092 | Hypersensitivity | |
| 124550922 | 12455092 | Laryngeal oedema | |
| 124550922 | 12455092 | Mouth swelling | |
| 124550922 | 12455092 | Swollen tongue |
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 |
|---|---|---|---|---|---|---|
| 124550922 | 12455092 | 1 | 20160523 | 0 | ||
| 124550922 | 12455092 | 2 | 20160523 | 0 | ||
| 124550922 | 12455092 | 3 | 20160523 | 0 |