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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125293922 | 12529392 | 2 | F | 20160621 | 20160706 | 20160706 | EXP | ES-JNJFOC-20160619120 | JOHNSON AND JOHNSON | BLANCA-LOPEZ N, PEREZ-ALZATE D, ANDREU I, DONA I, AGUNDEZ JA, GARCIA-MARTIN E, ET AL. IMMEDIATE HYPERSENSITIVITY REACTIONS TO IBUPROFEN AND OTHER ARYLPROPIONIC ACID DERIVATIVES. ALLERGY (EUROPEAN JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY) 2016;71 (7):1048-1056. | 36.00 | YR | A | F | Y | 0.00000 | 20160706 | OT | ES | ES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125293922 | 12529392 | 1 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | U | 0 | UNSPECIFIED | |||||||||
| 125293922 | 12529392 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | RECEIVED INCREMENTAL DOSES OF 5 MG, 50MG, 100MG, 150MG AND 300MG EVERY 60 MIN DURING ONE DAY. | U | 0 | UNSPECIFIED | ||||||||
| 125293922 | 12529392 | 3 | PS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | U | 19012 | UNSPECIFIED | |||||||||
| 125293922 | 12529392 | 4 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | RECEIVED INCREMENTAL DOSES OF 5 MG, 50MG, 100MG, 150MG AND 300MG EVERY 60 MIN DURING ONE DAY. | U | 19012 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125293922 | 12529392 | 1 | Drug provocation test |
| 125293922 | 12529392 | 2 | Drug provocation test |
| 125293922 | 12529392 | 3 | Product used for unknown indication |
| 125293922 | 12529392 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125293922 | 12529392 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125293922 | 12529392 | Anaphylactic shock | |
| 125293922 | 12529392 | Off label use | |
| 125293922 | 12529392 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |