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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126136824 | 12613682 | 4 | F | 20160829 | 20160802 | 20160831 | EXP | JP-009507513-1608JPN000043 | MERCK | 60.00 | YR | M | Y | 0.00000 | 20160831 | OT | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126136824 | 12613682 | 1 | PS | ESLAX INTRAVENOUS 25MG/2.5ML | ROCURONIUM BROMIDE | 1 | Intravenous (not otherwise specified) | 35 MG, QD | 20214 | 35 | MG | SOLUTION FOR INJECTION | QD | ||||||
| 126136824 | 12613682 | 2 | SS | PROPOFOL. | PROPOFOL | 1 | Parenteral | 70 MG, QD | 0 | 70 | MG | INFUSION | QD | ||||||
| 126136824 | 12613682 | 3 | SS | REMIFENTANIL HYDROCHLORIDE | REMIFENTANIL HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 0.4/MCG/KG/MIN, DAILY DOSE UNKNOWN | U | 0 | INJECTION | ||||||||
| 126136824 | 12613682 | 4 | SS | REMIFENTANIL HYDROCHLORIDE | REMIFENTANIL HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 0.1/MCG/KG/MIN, DAILY DOSE UNKNOWN | U | 0 | INJECTION | ||||||||
| 126136824 | 12613682 | 5 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Oral | 75 MG, QD. DIVIDED DOSE, FREQUENCY UNKNOWN | 0 | 75 | MG | ORAL POWDER | QD | ||||||
| 126136824 | 12613682 | 6 | C | SEVOFLURANE. | SEVOFLURANE | 1 | Respiratory (inhalation) | 0.5 %, DAILY DOSE UNKNOWN | 0 | INHALATION VAPOUR, SOLUTION | |||||||||
| 126136824 | 12613682 | 7 | C | SEVOFLURANE. | SEVOFLURANE | 1 | Respiratory (inhalation) | 0.6 %, DAILY DOSE UNKNOWN | 0 | INHALATION VAPOUR, SOLUTION | |||||||||
| 126136824 | 12613682 | 8 | C | SEVOFLURANE. | SEVOFLURANE | 1 | Respiratory (inhalation) | 0.5 %, DAILY DOSE UNKNOWN | 0 | INHALATION VAPOUR, SOLUTION | |||||||||
| 126136824 | 12613682 | 9 | C | EPHEDRINE HYDROCHLORIDE | EPHEDRINE HYDROCHLORIDE | 1 | Parenteral | 5MG X 5 TIMES, DAILY DOSE UNKNOWN | 0 | 15 | MG | INJECTION | |||||||
| 126136824 | 12613682 | 10 | C | EPHEDRINE HYDROCHLORIDE | EPHEDRINE HYDROCHLORIDE | 1 | Parenteral | 10 MG X TWICE, DAILY DOSE UNKNOWN | 0 | 20 | MG | INJECTION | |||||||
| 126136824 | 12613682 | 11 | C | NEOSYNESIN | PHENYLEPHRINE HYDROCHLORIDE | 1 | Parenteral | 0.1 MG X 3 TIMES, DAILY DOSE UNKNOWN | 0 | .3 | MG | INJECTION | |||||||
| 126136824 | 12613682 | 12 | C | NEOSYNESIN | PHENYLEPHRINE HYDROCHLORIDE | 1 | Parenteral | 0.2 MG, ONCE | 0 | .2 | MG | INJECTION | 1X | ||||||
| 126136824 | 12613682 | 13 | C | NEOSYNESIN | PHENYLEPHRINE HYDROCHLORIDE | 1 | Parenteral | 0.3 MG, ONCE | 0 | .3 | MG | INJECTION | 1X | ||||||
| 126136824 | 12613682 | 14 | C | ATROPINE SULFATE. | ATROPINE SULFATE | 1 | Parenteral | 0.5 MG, ONCE | 0 | .5 | MG | INJECTION | 1X | ||||||
| 126136824 | 12613682 | 15 | C | DOPAMINE | DOPAMINEDOPAMINE HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 3MCG/KG/MIN, DAILY DOSE UNKNOWN | 0 | INJECTION | |||||||||
| 126136824 | 12613682 | 16 | C | DOPAMINE | DOPAMINEDOPAMINE HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 5MCG/KG/MIN, DAILY DOSE UNKNOWN | 0 | INJECTION | |||||||||
| 126136824 | 12613682 | 17 | C | TELMISARTAN. | TELMISARTAN | 1 | Oral | DAILY DOSAGE UNKNOWN | 0 | ORAL POWDER |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126136824 | 12613682 | 1 | Neuromuscular blocking therapy |
| 126136824 | 12613682 | 2 | Induction of anaesthesia |
| 126136824 | 12613682 | 3 | Induction of anaesthesia |
| 126136824 | 12613682 | 6 | Maintenance of anaesthesia |
| 126136824 | 12613682 | 17 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126136824 | 12613682 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126136824 | 12613682 | Arteriospasm coronary | |
| 126136824 | 12613682 | Cardiac arrest |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |