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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126370301 | 12637030 | 1 | I | 20070623 | 20071210 | 20160809 | 20160809 | EXP | GB-ASTELLAS-2007002418 | ASTELLAS | 88.16 | YR | M | Y | 0.00000 | 20160809 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126370301 | 12637030 | 1 | PS | PLACEBO | UNSPECIFIED INGREDIENT | 1 | Oral | 23850 | MG | U | 0 | 150 | MG | FORMULATION UNKNOWN | QD | ||||
126370301 | 12637030 | 2 | C | PREDNISOLONE. | PREDNISOLONE | 1 | Oral | UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
126370301 | 12637030 | 3 | C | FOLIC ACID. | FOLIC ACID | 1 | Oral | U | 0 | 5 | MG | FORMULATION UNKNOWN | QD | ||||||
126370301 | 12637030 | 4 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Oral | U | 0 | 200 | MG | FORMULATION UNKNOWN | TID | ||||||
126370301 | 12637030 | 5 | C | SEREVENT DISKUS | SALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | UNK INHALANT, PRESSURISED, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
126370301 | 12637030 | 6 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | 250 MG, BD | U | 0 | 250 | MG | FORMULATION UNKNOWN | BID | |||||
126370301 | 12637030 | 7 | C | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Oral | U | 0 | 30 | MG | FORMULATION UNKNOWN | QD | ||||||
126370301 | 12637030 | 8 | C | SALBUTAMOL | ALBUTEROL | 1 | Respiratory (inhalation) | UNK, PRN | U | 0 | FORMULATION UNKNOWN | ||||||||
126370301 | 12637030 | 9 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Intravenous (not otherwise specified) | U | 0 | 500 | MG | FORMULATION UNKNOWN | |||||||
126370301 | 12637030 | 10 | C | HYDROXOCOBALAMIN | HYDROXOCOBALAMIN | 1 | Unknown | 1 MG, 3 MONTHLY | U | 0 | 1 | MG | FORMULATION UNKNOWN | ||||||
126370301 | 12637030 | 11 | C | COLLAGEN | COLLAGEN | 1 | Unknown | U | 0 | 200 | ML | FORMULATION UNKNOWN | |||||||
126370301 | 12637030 | 12 | C | NORMAL SALINE | SODIUM CHLORIDE | 1 | Unknown | 4 DEGREE PER LITRE, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126370301 | 12637030 | 1 | Non-small cell lung cancer |
126370301 | 12637030 | 2 | Product used for unknown indication |
126370301 | 12637030 | 3 | Product used for unknown indication |
126370301 | 12637030 | 4 | Product used for unknown indication |
126370301 | 12637030 | 5 | Product used for unknown indication |
126370301 | 12637030 | 6 | Product used for unknown indication |
126370301 | 12637030 | 7 | Product used for unknown indication |
126370301 | 12637030 | 8 | Product used for unknown indication |
126370301 | 12637030 | 9 | Product used for unknown indication |
126370301 | 12637030 | 10 | Product used for unknown indication |
126370301 | 12637030 | 11 | Product used for unknown indication |
126370301 | 12637030 | 12 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126370301 | 12637030 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126370301 | 12637030 | Anaemia | |
126370301 | 12637030 | Asthenia | |
126370301 | 12637030 | Dehydration | |
126370301 | 12637030 | Syncope |
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 |
---|---|---|---|---|---|---|
126370301 | 12637030 | 1 | 20070623 | 20071222 | 0 |