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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124632922 | 12463292 | 2 | F | 20160630 | 20160614 | 20160708 | EXP | US-MLMSERVICE-20160603-0308438-1 | US-STRIDES ARCOLAB LIMITED-2016SP006489 | STRIDES | 0.00 | Y | 0.00000 | 20160706 | OT | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124632922 | 12463292 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | UNK | U | U | 0 | |||||||||
| 124632922 | 12463292 | 2 | SS | FENTANYL. | FENTANYL | 1 | Intravenous (not otherwise specified) | 100 MCG, UNK | U | U | 0 | ||||||||
| 124632922 | 12463292 | 3 | SS | AZITHROMYCIN ANHYDROUS. | AZITHROMYCIN ANHYDROUS | 1 | UNK | U | U | 0 | |||||||||
| 124632922 | 12463292 | 4 | SS | MIDAZOLAM | MIDAZOLAMMIDAZOLAM HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 2 MG, UNK | 0 | 2 | MG | ||||||||
| 124632922 | 12463292 | 5 | SS | RHOGAM | HUMAN RHO(D) IMMUNE GLOBULIN | 1 | UNK | 0 | |||||||||||
| 124632922 | 12463292 | 6 | SS | COPPER | COPPER | 1 | Intra-uterine | UNK | 0 | IMPLANTATION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124632922 | 12463292 | 1 | Product used for unknown indication |
| 124632922 | 12463292 | 2 | Anaesthesia |
| 124632922 | 12463292 | 3 | Product used for unknown indication |
| 124632922 | 12463292 | 4 | Anaesthesia |
| 124632922 | 12463292 | 5 | Product used for unknown indication |
| 124632922 | 12463292 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124632922 | 12463292 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124632922 | 12463292 | Anaphylactic reaction | |
| 124632922 | 12463292 | Chest pain | |
| 124632922 | 12463292 | Dyspnoea | |
| 124632922 | 12463292 | Kounis syndrome | |
| 124632922 | 12463292 | Lactic acidosis | |
| 124632922 | 12463292 | Swelling face | |
| 124632922 | 12463292 | Urticaria |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |