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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127831801 | 12783180 | 1 | I | 20160718 | 20160913 | 20160927 | 20160927 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-124127 | RANBAXY | 19.00 | YR | M | Y | 82.55000 | KG | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127831801 | 12783180 | 1 | PS | FLUOXETINE | FLUOXETINE HYDROCHLORIDE | 1 | Oral | 20 MG, UNK | 76990 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127831801 | 12783180 | 1 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127831801 | 12783180 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127831801 | 12783180 | Abnormal dreams | |
| 127831801 | 12783180 | Anxiety | |
| 127831801 | 12783180 | Dyskinesia | |
| 127831801 | 12783180 | Dyspnoea | |
| 127831801 | 12783180 | Fatigue | |
| 127831801 | 12783180 | Feeling abnormal | |
| 127831801 | 12783180 | Flat affect | |
| 127831801 | 12783180 | Insomnia | |
| 127831801 | 12783180 | Memory impairment | |
| 127831801 | 12783180 | Panic attack | |
| 127831801 | 12783180 | Paraesthesia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |