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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126195021 | 12619502 | 1 | I | 20081023 | 20081104 | 20160803 | 20160803 | EXP | GB-ASTELLAS-2008002898 | ASTELLAS | 76.03 | YR | M | Y | 0.00000 | 20160803 | CN | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126195021 | 12619502 | 1 | PS | PLACEBO | UNSPECIFIED INGREDIENT | 1 | Oral | 94 | DF | 0 | 1 | DF | FORMULATION UNKNOWN | QD | |||||
126195021 | 12619502 | 2 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
126195021 | 12619502 | 3 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Oral | U | 0 | 50 | MG | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 4 | C | NIFEDIPINE. | NIFEDIPINE | 1 | Oral | U | 0 | 30 | MG | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 5 | C | ATENOLOL. | ATENOLOL | 1 | Oral | U | 0 | 25 | MG | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 6 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Oral | U | 0 | 1 | G | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 7 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | U | 0 | 40 | MG | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 8 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Oral | U | 0 | 200 | MG | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 9 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Respiratory (inhalation) | U | 0 | 18 | UG | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 10 | C | DEXAMETHASONE. | DEXAMETHASONE | 1 | Oral | U | 0 | 2 | MG | FORMULATION UNKNOWN | |||||||
126195021 | 12619502 | 11 | C | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Respiratory (inhalation) | REPORTED AS 200/6 | U | 0 | FORMULATION UNKNOWN | ||||||||
126195021 | 12619502 | 12 | C | CYCLIZINE | CYCLIZINE | 1 | Oral | U | 0 | 150 | MG | FORMULATION UNKNOWN |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126195021 | 12619502 | 1 | Non-small cell lung cancer |
126195021 | 12619502 | 2 | Product used for unknown indication |
126195021 | 12619502 | 3 | Product used for unknown indication |
126195021 | 12619502 | 4 | Product used for unknown indication |
126195021 | 12619502 | 5 | Product used for unknown indication |
126195021 | 12619502 | 6 | Product used for unknown indication |
126195021 | 12619502 | 7 | Product used for unknown indication |
126195021 | 12619502 | 8 | Product used for unknown indication |
126195021 | 12619502 | 9 | Product used for unknown indication |
126195021 | 12619502 | 10 | Product used for unknown indication |
126195021 | 12619502 | 11 | Product used for unknown indication |
126195021 | 12619502 | 12 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126195021 | 12619502 | DE |
126195021 | 12619502 | OT |
126195021 | 12619502 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126195021 | 12619502 | Blood calcium increased | |
126195021 | 12619502 | Non-small cell lung cancer |
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 |
---|---|---|---|---|---|---|
126195021 | 12619502 | 1 | 20080809 | 20081110 | 0 |