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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126848081 | 12684808 | 1 | I | 20160803 | 20160819 | 20160825 | 20160825 | EXP | GB-GLAXOSMITHKLINE-GB2016121330 | GLAXOSMITHKLINE | 87.00 | YR | F | Y | 0.00000 | 20160825 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126848081 | 12684808 | 1 | SS | Amitriptyline | AMITRIPTYLINE | 1 | Unknown | 100 MG, UNK | U | UNKNOWN | 0 | 100 | MG | ||||||
| 126848081 | 12684808 | 2 | SS | CLOPIDOGREL BISULFATE. | CLOPIDOGREL BISULFATE | 1 | Unknown | 75 MG, UNK | U | UNKNOWN | 0 | 75 | MG | ||||||
| 126848081 | 12684808 | 3 | SS | LACTULOSE. | LACTULOSE | 1 | Unknown | 15 ML, UNK | U | UNKNOWN | 0 | 15 | ML | ||||||
| 126848081 | 12684808 | 4 | SS | METOCLOPRAMIDE. | METOCLOPRAMIDE | 1 | Unknown | 10 MG, UNK | U | UNKNOWN | 0 | 10 | MG | ||||||
| 126848081 | 12684808 | 5 | SS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 5 MG, UNK | U | UNKNOWN | 0 | 5 | MG | ||||||
| 126848081 | 12684808 | 6 | PS | RANITIDINE. | RANITIDINE | 1 | Unknown | 300 MG, UNK | U | UNKNOWN | 18703 | 300 | MG | ||||||
| 126848081 | 12684808 | 7 | SS | LYRICA | PREGABALIN | 1 | Unknown | 150 MG, UNK | U | U | 0 | 150 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126848081 | 12684808 | 1 | Product used for unknown indication |
| 126848081 | 12684808 | 2 | Product used for unknown indication |
| 126848081 | 12684808 | 3 | Product used for unknown indication |
| 126848081 | 12684808 | 4 | Product used for unknown indication |
| 126848081 | 12684808 | 5 | Product used for unknown indication |
| 126848081 | 12684808 | 6 | Product used for unknown indication |
| 126848081 | 12684808 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126848081 | 12684808 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126848081 | 12684808 | Contusion | |
| 126848081 | 12684808 | Diarrhoea | |
| 126848081 | 12684808 | Loss of consciousness | |
| 126848081 | 12684808 | Skin abrasion |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |