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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127671511 | 12767151 | 1 | I | 20100607 | 20160915 | 20160921 | 20160921 | EXP | GB-MHRA-ADR 20645378 | GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK024324 | GLENMARK | 0.00 | Y | 0.00000 | 20160921 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127671511 | 12767151 | 1 | PS | EZETIMIBE. | EZETIMIBE | 1 | Oral | 10 MG, UNK | Y | 78560 | 10 | MG | |||||||
127671511 | 12767151 | 2 | I | Perindopril | PERINDOPRIL | 1 | Unknown | 4 MG, UNK | Y | 0 | 4 | MG | |||||||
127671511 | 12767151 | 3 | I | RANITIDINE HYDROCHLORIDE. | RANITIDINE HYDROCHLORIDE | 1 | Unknown | 150 MG, BID | Y | 0 | 150 | MG | BID | ||||||
127671511 | 12767151 | 4 | I | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | 20 MG, UNK | Y | 0 | 20 | MG | |||||||
127671511 | 12767151 | 5 | I | INDAPAMIDE. | INDAPAMIDE | 1 | Unknown | 2.5 MG, UNK | Y | 0 | 2.5 | MG | |||||||
127671511 | 12767151 | 6 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | Oral | 75 MG, UNK | 0 | 75 | MG | ||||||||
127671511 | 12767151 | 7 | C | GLICLAZIDE | GLICLAZIDE | 1 | Unknown | UNK | 0 | ||||||||||
127671511 | 12767151 | 8 | C | GLUCOSAMINE | GLUCOSAMINE | 1 | Oral | 100 MG, UNK | 0 | 100 | MG | ||||||||
127671511 | 12767151 | 9 | C | GTN | NITROGLYCERIN | 1 | Sublingual | 2 DF, UNK | 0 | 2 | DF | ||||||||
127671511 | 12767151 | 10 | C | TROLNITRATE PHOSPHATE | 2 | Unknown | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127671511 | 12767151 | 1 | Product used for unknown indication |
127671511 | 12767151 | 2 | Cerebrovascular accident prophylaxis |
127671511 | 12767151 | 3 | Cerebrovascular accident prophylaxis |
127671511 | 12767151 | 4 | Cerebrovascular accident prophylaxis |
127671511 | 12767151 | 5 | Cerebrovascular accident prophylaxis |
127671511 | 12767151 | 6 | Product used for unknown indication |
127671511 | 12767151 | 7 | Product used for unknown indication |
127671511 | 12767151 | 8 | Product used for unknown indication |
127671511 | 12767151 | 9 | Product used for unknown indication |
127671511 | 12767151 | 10 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127671511 | 12767151 | OT |
127671511 | 12767151 | HO |
127671511 | 12767151 | LT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127671511 | 12767151 | Drug interaction | |
127671511 | 12767151 | Hypotension | |
127671511 | 12767151 | Product use issue | |
127671511 | 12767151 | Stevens-Johnson syndrome |
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 |
---|---|---|---|---|---|---|
127671511 | 12767151 | 1 | 2010 | 0 | ||
127671511 | 12767151 | 2 | 2010 | 0 | ||
127671511 | 12767151 | 3 | 2010 | 0 | ||
127671511 | 12767151 | 4 | 2010 | 0 | ||
127671511 | 12767151 | 5 | 2010 | 0 |