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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127083111 | 12708311 | 1 | I | 20160818 | 20160826 | 20160901 | 20160901 | EXP | GB-MHRA-TPP10419171C2710752YC1471514489913 | GB-MYLANLABS-2016M1036854 | MYLAN | 0.00 | Y | 0.00000 | 20160901 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127083111 | 12708311 | 1 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 40 MG, UNK | U | 90868 | 40 | MG | |||||||
127083111 | 12708311 | 2 | C | BETAHISTINE | BETAHISTINE | 1 | 1 DF, TID | 719.875 | DF | U | 0 | 1 | DF | TID | |||||
127083111 | 12708311 | 3 | C | BUDESONIDE. | BUDESONIDE | 1 | UNK (USE AS DIRECTED) | U | 0 | ||||||||||
127083111 | 12708311 | 4 | C | SALBUTAMOL | ALBUTEROL | 1 | Respiratory (inhalation) | 2 DF, UNK | U | 0 | 2 | DF |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127083111 | 12708311 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127083111 | 12708311 | Pain |
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 |
---|---|---|---|---|---|---|
127083111 | 12708311 | 1 | 20160818 | 0 | ||
127083111 | 12708311 | 2 | 20151222 | 0 | ||
127083111 | 12708311 | 3 | 20150715 | 0 | ||
127083111 | 12708311 | 4 | 20150715 | 0 |