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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127079671 | 12707967 | 1 | I | 20160619 | 20160826 | 20160901 | 20160901 | EXP | FR-PFIZER INC-2016405816 | PFIZER | 12.00 | YR | F | Y | 0.00000 | 20160901 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127079671 | 12707967 | 1 | PS | Fragmine | DALTEPARIN SODIUM | 1 | Subcutaneous | 1 DF OF 2500 IU ANTI XA/0.2 ML, 1X/DAY | Y | 20287 | 2500 | IU | SOLUTION FOR INJECTION | QD | |||||
| 127079671 | 12707967 | 2 | SS | PROPOFOL LIPURO | PROPOFOL | 1 | Epidural | 100 MG AND 50 MG, SINGLE | 0 | 150 | MG | EMULSION FOR INJECTION | |||||||
| 127079671 | 12707967 | 3 | SS | PROFENID | KETOPROFEN | 1 | Intravenous (not otherwise specified) | 1 MG/KG, SINGLE | 0 | 1 | MG/KG | POWDER FOR SOLUTION FOR INJECTION | |||||||
| 127079671 | 12707967 | 4 | SS | SUFENTANIL | SUFENTANIL | 1 | Epidural | 10 UG + 5 UG + 5 UG, SINGLE | 0 | 20 | UG | ||||||||
| 127079671 | 12707967 | 5 | SS | KETAMINE RENAUDIN | KETAMINE | 1 | Epidural | 10 MG, 1X/DAY | 10 | MG | 0 | 10 | MG | SOLUTION FOR INJECTION | QD | ||||
| 127079671 | 12707967 | 6 | SS | PARACETAMOL MACOPHARMA | ACETAMINOPHEN | 1 | Intravenous (not otherwise specified) | 15 MG/KG, 4X/DAY EVERY 6 HOURS | 240 | MG/KG | Y | 0 | 15 | MG/KG | QID | ||||
| 127079671 | 12707967 | 7 | SS | ONDANSETRON ACCORD | ONDANSETRON | 1 | Intravenous (not otherwise specified) | 0.1 MG/KG, 3X/DAY EVERY 8 HOURS | 1.6 | MG/KG | Y | 0 | .1 | MG/KG | TID | ||||
| 127079671 | 12707967 | 8 | SS | CHIROCAINE | LEVOBUPIVACAINE HYDROCHLORIDE | 1 | Epidural | 7.5 MG + 10 MG + 15 MG + 0.05 MG, EVERY HOURS | 0 | 32.55 | MG | ||||||||
| 127079671 | 12707967 | 9 | SS | NALBUPHINE | NALBUPHINE | 1 | Intravenous (not otherwise specified) | 7 MG, SINGLE | 0 | 7 | MG | SOLUTION FOR INJECTION | |||||||
| 127079671 | 12707967 | 10 | SS | CEFAZOLINE MYLAN | CEFAZOLIN SODIUM | 1 | Intravenous (not otherwise specified) | 12.5 MG/KG, 3X/DAY EVERY 8 HOURS | 75 | MG/KG | 0 | 12.5 | MG/KG | POWDER FOR SOLUTION FOR INJECTION | TID | ||||
| 127079671 | 12707967 | 11 | SS | DROPERIDOL AGUETTANT | DROPERIDOL | 1 | Intravenous (not otherwise specified) | 1 MG, 4X/DAY EVERY 6 HOURS | 12 | MG | Y | 0 | 1 | MG | SOLUTION FOR INJECTION | QID | |||
| 127079671 | 12707967 | 12 | C | EUPANTOL | PANTOPRAZOLE SODIUM | 1 | UNK | 0 | |||||||||||
| 127079671 | 12707967 | 13 | C | CALCIDOSE VITAMINE D | CALCIUMCHOLECALCIFEROL | 1 | UNK | 0 | ORAL POWDER | ||||||||||
| 127079671 | 12707967 | 14 | C | DIFFU K | POTASSIUM CHLORIDE | 1 | UNK | 0 | |||||||||||
| 127079671 | 12707967 | 15 | C | ELUDRIL /02860401/ | CHLORHEXIDINE GLUCONATECHLOROBUTANOL | 1 | UNK | 0 | |||||||||||
| 127079671 | 12707967 | 16 | C | FUNGIZONE | AMPHOTERICIN B | 1 | UNK | 0 | |||||||||||
| 127079671 | 12707967 | 17 | C | MORPHINE | MORPHINE | 1 | UNK | 0 | |||||||||||
| 127079671 | 12707967 | 18 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | UNK | 0 | |||||||||||
| 127079671 | 12707967 | 19 | C | PHOSPHONEUROS | CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSMAGNESIUM GLYCEROPHOSPHATEPHOSPHORIC ACIDSODIUM PHOSPHATE, DIBASIC | 1 | UNK | 0 | |||||||||||
| 127079671 | 12707967 | 20 | C | UVEDOSE | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127079671 | 12707967 | 1 | Anticoagulant therapy |
| 127079671 | 12707967 | 2 | Anaesthesia |
| 127079671 | 12707967 | 3 | Analgesic therapy |
| 127079671 | 12707967 | 4 | Anaesthesia |
| 127079671 | 12707967 | 5 | Anaesthesia |
| 127079671 | 12707967 | 6 | Analgesic therapy |
| 127079671 | 12707967 | 7 | Antiemetic supportive care |
| 127079671 | 12707967 | 8 | Anaesthesia |
| 127079671 | 12707967 | 9 | Analgesic therapy |
| 127079671 | 12707967 | 10 | Antibiotic prophylaxis |
| 127079671 | 12707967 | 11 | Prophylaxis of nausea and vomiting |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127079671 | 12707967 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127079671 | 12707967 | Cholelithiasis | |
| 127079671 | 12707967 | Pancreatic necrosis | |
| 127079671 | 12707967 | Pancreatitis acute |
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 |
|---|---|---|---|---|---|---|
| 127079671 | 12707967 | 1 | 20160618 | 0 | ||
| 127079671 | 12707967 | 2 | 20160616 | 20160616 | 0 | |
| 127079671 | 12707967 | 3 | 20160618 | 20160618 | 0 | |
| 127079671 | 12707967 | 4 | 20160616 | 20160616 | 0 | |
| 127079671 | 12707967 | 5 | 20160616 | 20160616 | 0 | |
| 127079671 | 12707967 | 6 | 20160616 | 20160620 | 0 | |
| 127079671 | 12707967 | 7 | 20160616 | 20160620 | 0 | |
| 127079671 | 12707967 | 8 | 20160616 | 20160717 | 0 | |
| 127079671 | 12707967 | 9 | 20160616 | 20160616 | 0 | |
| 127079671 | 12707967 | 10 | 20160616 | 20160617 | 0 | |
| 127079671 | 12707967 | 11 | 20160617 | 20160620 | 0 |