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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126837591 | 12683759 | 1 | I | 20160601 | 20160810 | 20160825 | 20160825 | EXP | MP20160889 | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002495 | VALIDUS | 0.00 | M | Y | 0.00000 | 20160825 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126837591 | 12683759 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 40 MG, QD | U | 16273 | 40 | MG | |||||||
| 126837591 | 12683759 | 2 | SS | CEFOTAXIME SODIUM | CEFOTAXIME SODIUM | 1 | Intravenous (not otherwise specified) | 33 MG/KG, UNK | U | 0 | 33 | MG/KG | |||||||
| 126837591 | 12683759 | 3 | SS | CORTANCYL | PREDNISONE | 1 | Oral | 2 MG/KG, QD | U | 0 | 2 | MG/KG | |||||||
| 126837591 | 12683759 | 4 | SS | TAVANIC | LEVOFLOXACIN | 1 | UNK | U | 0 | ||||||||||
| 126837591 | 12683759 | 5 | SS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous (not otherwise specified) | 1 MG/KG, UNK | 0 | 1 | MG/KG | ||||||||
| 126837591 | 12683759 | 6 | SS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous (not otherwise specified) | 35 MG, BID | 0 | 35 | MG | ||||||||
| 126837591 | 12683759 | 7 | SS | KETAMINE | KETAMINE | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
| 126837591 | 12683759 | 8 | SS | CELOCURINE | SUCCINYLCHOLINE CHLORIDE | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
| 126837591 | 12683759 | 9 | SS | NIMBEX | CISATRACURIUM BESYLATE | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
| 126837591 | 12683759 | 10 | SS | SALBUTAMOL | ALBUTEROL | 1 | Intravenous (not otherwise specified) | 1.8 ?G, QD | U | 0 | 1.8 | UG | |||||||
| 126837591 | 12683759 | 11 | SS | SALBUTAMOL | ALBUTEROL | 1 | 5 ?G; EVERY HOUR; INHALATIONAL | U | 0 | 5 | UG | ||||||||
| 126837591 | 12683759 | 12 | SS | ATROVENT | IPRATROPIUM BROMIDE | 1 | 0.25 MG, EVERY 3 HOURS; INHALATIONAL | U | 0 | .25 | MG | ||||||||
| 126837591 | 12683759 | 13 | SS | LOXEN /00639802/ | NICARDIPINE | 1 | Oral | UNK | U | 0 | |||||||||
| 126837591 | 12683759 | 14 | SS | CIFLOX /00697201/ | CIPROFLOXACIN | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
| 126837591 | 12683759 | 15 | SS | MAGNESIUM SULFATE. | MAGNESIUM SULFATE | 1 | Intravenous (not otherwise specified) | 50 MG/KG, QD | Y | 0 | 50 | MG/KG | |||||||
| 126837591 | 12683759 | 16 | C | VENTOLINE /00139501/ | ALBUTEROL | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126837591 | 12683759 | 1 | Product used for unknown indication |
| 126837591 | 12683759 | 2 | Product used for unknown indication |
| 126837591 | 12683759 | 3 | Product used for unknown indication |
| 126837591 | 12683759 | 4 | Product used for unknown indication |
| 126837591 | 12683759 | 5 | Product used for unknown indication |
| 126837591 | 12683759 | 7 | Product used for unknown indication |
| 126837591 | 12683759 | 8 | Product used for unknown indication |
| 126837591 | 12683759 | 9 | Product used for unknown indication |
| 126837591 | 12683759 | 10 | Product used for unknown indication |
| 126837591 | 12683759 | 12 | Product used for unknown indication |
| 126837591 | 12683759 | 13 | Product used for unknown indication |
| 126837591 | 12683759 | 14 | Product used for unknown indication |
| 126837591 | 12683759 | 15 | Product used for unknown indication |
| 126837591 | 12683759 | 16 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126837591 | 12683759 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126837591 | 12683759 | Altered state of consciousness | |
| 126837591 | 12683759 | Cerebrovascular accident | |
| 126837591 | 12683759 | Cerebrovascular disorder |
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 |
|---|---|---|---|---|---|---|
| 126837591 | 12683759 | 1 | 20160526 | 20160526 | 0 | |
| 126837591 | 12683759 | 2 | 20160527 | 0 | ||
| 126837591 | 12683759 | 3 | 20160526 | 20160526 | 0 | |
| 126837591 | 12683759 | 4 | 20160527 | 0 | ||
| 126837591 | 12683759 | 5 | 20160527 | 0 | ||
| 126837591 | 12683759 | 6 | 2016 | 0 | ||
| 126837591 | 12683759 | 7 | 20160527 | 20160531 | 0 | |
| 126837591 | 12683759 | 8 | 20160527 | 20160527 | 0 | |
| 126837591 | 12683759 | 9 | 20160527 | 20160531 | 0 | |
| 126837591 | 12683759 | 10 | 20160527 | 20160530 | 0 | |
| 126837591 | 12683759 | 11 | 20160527 | 0 | ||
| 126837591 | 12683759 | 12 | 20160527 | 0 | ||
| 126837591 | 12683759 | 13 | 20160531 | 0 | ||
| 126837591 | 12683759 | 14 | 20160531 | 0 | ||
| 126837591 | 12683759 | 15 | 20160527 | 0 |