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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127416041 | 12741604 | 1 | I | 20160730 | 20160830 | 20160914 | 20160914 | EXP | FR-PFM-FR-2016-2596 | PIERRE FABRE MEDICAMENT | 71.31 | YR | F | Y | 0.00000 | 20160914 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127416041 | 12741604 | 1 | PS | NAVELBINE | VINORELBINE TARTRATE | 1 | Oral | CYCLICAL ADMINISTRATION (NOS) | Y | 0 | CAPSULE, SOFT | ||||||||
| 127416041 | 12741604 | 2 | SS | Cisplatin Accord | CISPLATIN | 1 | Intravenous (not otherwise specified) | CYCLICAL ADMINISTRATION (NOS) | Y | 0 | |||||||||
| 127416041 | 12741604 | 3 | C | Atorvastatine | ATORVASTATIN | 1 | Unknown | U | U | 0 | |||||||||
| 127416041 | 12741604 | 4 | C | Inexium | ESOMEPRAZOLE | 1 | Unknown | U | U | 0 | |||||||||
| 127416041 | 12741604 | 5 | C | MICARDIS | TELMISARTAN | 1 | Unknown | U | U | 0 | |||||||||
| 127416041 | 12741604 | 6 | C | Lercanidipine | LERCANIDIPINE | 1 | Unknown | U | U | 0 | |||||||||
| 127416041 | 12741604 | 7 | C | Paracetamol | ACETAMINOPHEN | 1 | Unknown | U | U | 0 | |||||||||
| 127416041 | 12741604 | 8 | C | Zophren | ONDANSETRON | 1 | Unknown | U | U | 0 | |||||||||
| 127416041 | 12741604 | 9 | C | EMEND | APREPITANT | 1 | Unknown | U | U | 0 | |||||||||
| 127416041 | 12741604 | 10 | C | PRIMPERAN | METOCLOPRAMIDE HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 127416041 | 12741604 | 11 | C | Cortancyl | PREDNISONE | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127416041 | 12741604 | 1 | Lung carcinoma cell type unspecified stage II |
| 127416041 | 12741604 | 2 | Lung carcinoma cell type unspecified stage II |
| 127416041 | 12741604 | 3 | Product used for unknown indication |
| 127416041 | 12741604 | 4 | Product used for unknown indication |
| 127416041 | 12741604 | 5 | Product used for unknown indication |
| 127416041 | 12741604 | 6 | Product used for unknown indication |
| 127416041 | 12741604 | 7 | Product used for unknown indication |
| 127416041 | 12741604 | 8 | Product used for unknown indication |
| 127416041 | 12741604 | 9 | Product used for unknown indication |
| 127416041 | 12741604 | 10 | Product used for unknown indication |
| 127416041 | 12741604 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127416041 | 12741604 | LT |
| 127416041 | 12741604 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127416041 | 12741604 | Arterial thrombosis | |
| 127416041 | 12741604 | Atrial fibrillation | |
| 127416041 | 12741604 | Bone marrow failure | |
| 127416041 | 12741604 | Decreased appetite | |
| 127416041 | 12741604 | Diarrhoea | |
| 127416041 | 12741604 | Intestinal infarction | |
| 127416041 | 12741604 | Nausea | |
| 127416041 | 12741604 | Neutropenia | |
| 127416041 | 12741604 | Vomiting | |
| 127416041 | 12741604 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 127416041 | 12741604 | 1 | 20160719 | 20160730 | 0 | |
| 127416041 | 12741604 | 2 | 20160719 | 20160720 | 0 |