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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122982083 | 12298208 | 3 | F | 20160202 | 20160901 | 20160423 | 20160913 | EXP | GB-MHRA-ADR 23419228 | GB-ACCORD-039769 | ACCORD | 72.00 | YR | F | Y | 0.00000 | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122982083 | 12298208 | 1 | PS | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Oral | ALSO RECEIVED CLOPIDOGREL PREVIOUSLY FROM DEC-2014 | 202925 | 75 | MG | QD | |||||||
| 122982083 | 12298208 | 2 | I | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | Y | 112044 | 40 | MG | ||||||||
| 122982083 | 12298208 | 3 | C | ALENDRONATE SODIUM/ALENDRONIC ACID | 2 | 0 | |||||||||||||
| 122982083 | 12298208 | 4 | C | REFRESH CELLUVISC | CARBOXYMETHYLCELLULOSE SODIUM | 1 | 0 | ||||||||||||
| 122982083 | 12298208 | 5 | C | EZETIMIBE. | EZETIMIBE | 1 | 0 | ||||||||||||
| 122982083 | 12298208 | 6 | C | LATANOPROST. | LATANOPROST | 1 | 0 | ||||||||||||
| 122982083 | 12298208 | 7 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | 0 | ||||||||||||
| 122982083 | 12298208 | 8 | C | RAMIPRIL. | RAMIPRIL | 1 | 0 | 10 | MG | QD | |||||||||
| 122982083 | 12298208 | 9 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | 0 | ||||||||||||
| 122982083 | 12298208 | 10 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | 0 | ||||||||||||
| 122982083 | 12298208 | 11 | C | ACETYLSALICYLIC ACID | ASPIRIN | 1 | 0 | 300 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122982083 | 12298208 | 1 | Thrombosis prophylaxis |
| 122982083 | 12298208 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122982083 | 12298208 | OT |
| 122982083 | 12298208 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122982083 | 12298208 | Facial paralysis | |
| 122982083 | 12298208 | Labelled drug-drug interaction medication error | |
| 122982083 | 12298208 | Transient ischaemic attack | |
| 122982083 | 12298208 | Treatment failure |
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 |
|---|---|---|---|---|---|---|
| 122982083 | 12298208 | 1 | 201503 | 0 | ||
| 122982083 | 12298208 | 2 | 20150301 | 20160202 | 0 |