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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126171011 | 12617101 | 1 | I | 20160712 | 20160803 | 20160803 | EXP | GB-CIPLA LTD.-2016GB09875 | CIPLA | 0.00 | Y | 0.00000 | 20160803 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126171011 | 12617101 | 1 | PS | NAPROXEN. | NAPROXEN | 1 | Unknown | 500 MG, BID | U | 91305 | 500 | MG | TABLET | BID | |||||
| 126171011 | 12617101 | 2 | SS | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Unknown | 75 MG, QD, MORNING | U | 0 | 75 | MG | QD | ||||||
| 126171011 | 12617101 | 3 | C | Atorvastatin | ATORVASTATIN | 1 | Unknown | 40 MG, QD, AT NIGHT | U | U | 0 | 40 | MG | QD | |||||
| 126171011 | 12617101 | 4 | C | Betahistine | BETAHISTINE | 1 | Unknown | 8 MG, TID | U | U | 0 | 8 | MG | ||||||
| 126171011 | 12617101 | 5 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Unknown | 200 MG, QD | U | U | 0 | 200 | MG | QD | |||||
| 126171011 | 12617101 | 6 | C | LACTULOSE. | LACTULOSE | 1 | Oral | 15 ML, BID, 3.1-3.7 G/5ML, 8 AM AND 10 PM | U | U | 0 | 15 | ML | BID | |||||
| 126171011 | 12617101 | 7 | C | LEVETIRACETAM. | LEVETIRACETAM | 1 | Unknown | 1 G, BID | U | U | 0 | 1 | G | BID | |||||
| 126171011 | 12617101 | 8 | C | Quinine | QUININE | 1 | Unknown | 300 MG, QD, AT NIGHT | U | U | 0 | 300 | MG | QD | |||||
| 126171011 | 12617101 | 9 | C | EPILIM | VALPROATE SODIUM | 1 | Unknown | 500 MG, BID | U | U | 0 | 500 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126171011 | 12617101 | 1 | Back pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126171011 | 12617101 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126171011 | 12617101 | Abdominal pain | |
| 126171011 | 12617101 | Back pain | |
| 126171011 | 12617101 | Gastrointestinal haemorrhage | |
| 126171011 | 12617101 | Haematemesis |
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 |
|---|---|---|---|---|---|---|
| 126171011 | 12617101 | 1 | 20160214 | 0 |