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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125810181 | 12581018 | 1 | I | 201510 | 20151124 | 20160721 | 20160721 | PER | US-APOTEX-2015AP014916 | APOTEX | 60.01 | YR | F | Y | 64.00000 | KG | 20160721 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125810181 | 12581018 | 1 | PS | ATORVASTATIN CALCIUM. | ATORVASTATIN CALCIUM | 1 | Oral | 10 MG, ON MONDAY, WEDNESDAY AND FRIDAY | Y | 90548 | 10 | MG | TABLET | ||||||
| 125810181 | 12581018 | 2 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | 800 MG, AS NEEDED | U | U | 0 | 800 | MG | ||||||
| 125810181 | 12581018 | 3 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | Oral | U | U | 06H D19839, DAC 02013, 434803-03 | 0 | ||||||||
| 125810181 | 12581018 | 4 | C | OMEGA /00661201/ | 2 | Unknown | U | U | 0 | ||||||||||
| 125810181 | 12581018 | 5 | C | SUPER B COMPLEX /01995301/ | CYANOCOBALAMINDEXPANTHENOLNIACINAMIDEPYRIDOXINE HYDROCHLORIDERIBOFLAVIN 5'-PHOSPHATE SODIUMTHIAMINE HYDROCHLORIDEVITAMIN B COMPLEX | 1 | Unknown | BIOTIN- VITAMIN C 50MG +FOLIC ACID 400MG +B12 25MG +B6 8MG +BIOTIN L200MCG, ONE TABLET ONCE A DAY | U | U | 13168, 931417-02 | 0 | |||||||
| 125810181 | 12581018 | 6 | C | COENZYME Q10 | UBIDECARENONE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125810181 | 12581018 | 7 | C | VITAMIN B12 | CYANOCOBALAMIN | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125810181 | 12581018 | 8 | C | VITAMIN C | ASCORBIC ACID | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125810181 | 12581018 | 9 | C | VITAMIN D /00107901/ | ERGOCALCIFEROL | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125810181 | 12581018 | 10 | C | FIORICET | ACETAMINOPHENBUTALBITALCAFFEINE | 1 | Unknown | 1 OR 2X PER MONTH ONLY AS NEEDED | U | U | 0 | ||||||||
| 125810181 | 12581018 | 11 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Unknown | 1X OR 2X PER MONTH | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125810181 | 12581018 | 1 | Hyperlipidaemia |
| 125810181 | 12581018 | 2 | Pain |
| 125810181 | 12581018 | 3 | Vitamin D decreased |
| 125810181 | 12581018 | 4 | Product used for unknown indication |
| 125810181 | 12581018 | 5 | Product used for unknown indication |
| 125810181 | 12581018 | 6 | Product used for unknown indication |
| 125810181 | 12581018 | 7 | Product used for unknown indication |
| 125810181 | 12581018 | 8 | Product used for unknown indication |
| 125810181 | 12581018 | 9 | Product used for unknown indication |
| 125810181 | 12581018 | 10 | Product used for unknown indication |
| 125810181 | 12581018 | 11 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125810181 | 12581018 | Headache | |
| 125810181 | 12581018 | Nausea | |
| 125810181 | 12581018 | Pain of skin | |
| 125810181 | 12581018 | Pyrexia |
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 |
|---|---|---|---|---|---|---|
| 125810181 | 12581018 | 1 | 20150929 | 201510 | 0 | |
| 125810181 | 12581018 | 2 | 2013 | 0 | ||
| 125810181 | 12581018 | 6 | 2012 | 0 | ||
| 125810181 | 12581018 | 7 | 2005 | 0 | ||
| 125810181 | 12581018 | 8 | 2005 | 0 | ||
| 125810181 | 12581018 | 9 | 2005 | 0 | ||
| 125810181 | 12581018 | 10 | 2000 | 0 | ||
| 125810181 | 12581018 | 11 | 2005 | 0 |