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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126015694 | 12601569 | 4 | F | 20160711 | 20160822 | 20160728 | 20160831 | EXP | GB-DRREDDYS-GER/UKI/16/0081737 | DR REDDYS | 77.00 | YR | F | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126015694 | 12601569 | 1 | PS | Atorvastatin | ATORVASTATIN | 1 | U | U | UNKNOWN | 91650 | |||||||||
| 126015694 | 12601569 | 2 | SS | MONTELUKAST | MONTELUKAST SODIUM | 1 | U | U | 201582 | ||||||||||
| 126015694 | 12601569 | 3 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | U | U | 75576 | ||||||||||
| 126015694 | 12601569 | 4 | SS | PREGABALIN. | PREGABALIN | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 5 | SS | BETAHISTINE | BETAHISTINE | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 6 | SS | BISOPROLOL | BISOPROLOL | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 7 | SS | ELIQUIS | APIXABAN | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 8 | SS | FERROUS GLUCONATE | FERROUS GLUCONATE | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 9 | SS | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 10 | SS | LINAGLIPTIN | LINAGLIPTIN | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 11 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 12 | SS | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 13 | SS | THIAMINE. | THIAMINE | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 14 | SS | ZOPICLONE | ZOPICLONE | 1 | U | U | 0 | ||||||||||
| 126015694 | 12601569 | 15 | C | UMECLIDINIUM | UMECLIDINIUM BROMIDE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126015694 | 12601569 | 1 | Product used for unknown indication |
| 126015694 | 12601569 | 2 | Product used for unknown indication |
| 126015694 | 12601569 | 3 | Product used for unknown indication |
| 126015694 | 12601569 | 4 | Product used for unknown indication |
| 126015694 | 12601569 | 5 | Product used for unknown indication |
| 126015694 | 12601569 | 6 | Product used for unknown indication |
| 126015694 | 12601569 | 7 | Product used for unknown indication |
| 126015694 | 12601569 | 8 | Product used for unknown indication |
| 126015694 | 12601569 | 9 | Product used for unknown indication |
| 126015694 | 12601569 | 10 | Product used for unknown indication |
| 126015694 | 12601569 | 11 | Product used for unknown indication |
| 126015694 | 12601569 | 12 | Product used for unknown indication |
| 126015694 | 12601569 | 13 | Product used for unknown indication |
| 126015694 | 12601569 | 14 | Product used for unknown indication |
| 126015694 | 12601569 | 15 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126015694 | 12601569 | OT |
| 126015694 | 12601569 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126015694 | 12601569 | Cough | |
| 126015694 | 12601569 | Lethargy | |
| 126015694 | 12601569 | Sputum discoloured | |
| 126015694 | 12601569 | Toxic skin eruption | |
| 126015694 | 12601569 | Viral rash |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |