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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127456531 | 12745653 | 1 | I | 20150401 | 20160902 | 20160915 | 20160915 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123743 | RANBAXY | 64.00 | YR | M | Y | 88.00000 | KG | 20160915 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127456531 | 12745653 | 1 | PS | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 150 MG, UNK | Y | U | SEVERAL | 91272 | 150 | MG | |||||
| 127456531 | 12745653 | 2 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | U | U | 0 | |||||||||
| 127456531 | 12745653 | 3 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Unknown | U | U | 0 | |||||||||
| 127456531 | 12745653 | 4 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | U | U | 0 | |||||||||
| 127456531 | 12745653 | 5 | C | RAMIPRIL. | RAMIPRIL | 1 | Unknown | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127456531 | 12745653 | 1 | Antidepressant therapy |
| 127456531 | 12745653 | 2 | Product used for unknown indication |
| 127456531 | 12745653 | 3 | Product used for unknown indication |
| 127456531 | 12745653 | 4 | Product used for unknown indication |
| 127456531 | 12745653 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127456531 | 12745653 | OT |
| 127456531 | 12745653 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127456531 | 12745653 | Acrophobia | |
| 127456531 | 12745653 | Asthenia | |
| 127456531 | 12745653 | Diarrhoea | |
| 127456531 | 12745653 | Dizziness | |
| 127456531 | 12745653 | Drug ineffective | |
| 127456531 | 12745653 | Drug withdrawal headache | |
| 127456531 | 12745653 | Drug withdrawal syndrome | |
| 127456531 | 12745653 | Influenza like illness | |
| 127456531 | 12745653 | Insomnia | |
| 127456531 | 12745653 | Myalgia | |
| 127456531 | 12745653 | Nightmare | |
| 127456531 | 12745653 | Product substitution issue | |
| 127456531 | 12745653 | Psychiatric symptom | |
| 127456531 | 12745653 | Tinnitus |
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 |
|---|---|---|---|---|---|---|
| 127456531 | 12745653 | 1 | 20110101 | 20150605 | 0 |