Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542788 | 4126153 | F | 4542788-5 | 20030212 | 20040405 | 20041231 | EXP | PHHO2004JP05093 | NOVARTIS PHARMACEUTICALS CORP. | 74 | YR | F | Y | 50 | KG | 20041231 | MD |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542788 | 1005547049 | PS | DIOVAN | 1 | ORAL | 80 MG, QD | |||||
| 4542788 | 1005547050 | C | LIPITOR | 1 | ORAL | 10 MG, | |||||
| 4542788 | 1005547051 | C | CHOLEBRINE | 1 | ORAL | 3 G, | |||||
| 4542788 | 1005547052 | C | HUMACART-N | 2 | SUBCUTANEOUS | 25LU |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4542788 | 1005547049 | HYPERTENSION |
| 4542788 | 1005547050 | HYPERCHOLESTEROLAEMIA |
| 4542788 | 1005547051 | HYPERCHOLESTEROLAEMIA |
| 4542788 | 1005547052 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542788 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4542788 | CAROTID ARTERY DISEASE |
| 4542788 | DISEASE PROGRESSION |
| 4542788 | NAUSEA |
| 4542788 | REFLUX OESOPHAGITIS |
| 4542788 | RENAL IMPAIRMENT |
| 4542788 | TRANSIENT ISCHAEMIC ATTACK |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4542788 | 1005547049 | 20021202 | |||
| 4542788 | 1005547050 | 20020527 | |||
| 4542788 | 1005547051 | 20020122 | |||
| 4542788 | 1005547052 | 20020122 |