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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126489914 | 12648991 | 4 | F | 20160712 | 20160818 | 20160812 | 20160831 | EXP | GB-MHRA-EYC 00143286 | GB-PFIZER INC-2016379090 | PFIZER | 88.00 | YR | M | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126489914 | 12648991 | 1 | PS | SERTRALINE HCL | SERTRALINE HYDROCHLORIDE | 1 | Oral | 50 MG, 1X/DAY | 19839 | 50 | MG | QD | |||||||
| 126489914 | 12648991 | 2 | SS | APIXABAN | APIXABAN | 1 | Oral | 2.5 MG, 2X/DAY | Y | 0 | 2.5 | MG | FILM-COATED TABLET | BID | |||||
| 126489914 | 12648991 | 3 | C | ATORVASTATIN | ATORVASTATIN | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 4 | C | BISOPROLOL | BISOPROLOL | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 5 | C | CHLORAMPHENICOL | CHLORAMPHENICOL | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 6 | C | DEXTROSE. | DEXTROSE | 1 | UNK | 0 | GEL | ||||||||||
| 126489914 | 12648991 | 7 | C | DIGOXIN. | DIGOXIN | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 8 | C | FERROUS FUMARATE | FERROUS FUMARATE | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 9 | C | GLICLAZIDE | GLICLAZIDE | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 10 | C | ISOTARD XL | 2 | UNK | 0 | ||||||||||||
| 126489914 | 12648991 | 11 | C | LACTULOSE. | LACTULOSE | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 12 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 13 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 14 | C | RAMIPRIL. | RAMIPRIL | 1 | UNK | 0 | |||||||||||
| 126489914 | 12648991 | 15 | C | PARACETAMOL | ACETAMINOPHEN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126489914 | 12648991 | 1 | Depression |
| 126489914 | 12648991 | 2 | Cerebrovascular accident prophylaxis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126489914 | 12648991 | HO |
| 126489914 | 12648991 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126489914 | 12648991 | Abdominal pain | |
| 126489914 | 12648991 | Abnormal faeces | |
| 126489914 | 12648991 | Asthenia | |
| 126489914 | 12648991 | Dysphagia | |
| 126489914 | 12648991 | Faeces discoloured | |
| 126489914 | 12648991 | Haematemesis | |
| 126489914 | 12648991 | Pneumonia aspiration | |
| 126489914 | 12648991 | Upper gastrointestinal haemorrhage |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |