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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5742248 | 6626179 | F | 5742248-X | 20080509 | 20080519 | EXP | PHHY2008ZA06159 | NOVARTIS PHARMACEUTICALS CORP. | 89 | YR | M | Y | 20080517 | OT | SOUTH AFRICA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5742248 | 1009923974 | C | TRANQIPAM | 2 | |||||||
| 5742248 | 1009923975 | C | LENTOGESIC /01351301/ | 2 | |||||||
| 5742248 | 1009923976 | C | AVELON | 2 | |||||||
| 5742248 | 1009923977 | PS | ZOMETA | 1 | 4MG POWDER FOR SOLUTION | 021223 | |||||
| 5742248 | 1009923978 | SS | ZOMETA | 1 | 021223 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5742248 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5742248 | BLOOD ALBUMIN DECREASED |
| 5742248 | BLOOD CALCIUM DECREASED |
| 5742248 | CONFUSIONAL STATE |
| 5742248 | DELUSIONAL DISORDER, UNSPECIFIED TYPE |
| 5742248 | FATIGUE |
| 5742248 | HAEMATOCRIT DECREASED |
| 5742248 | HAEMOGLOBIN DECREASED |
| 5742248 | MONOCYTE COUNT ABNORMAL |
| 5742248 | NAUSEA |
| 5742248 | PROSTATIC SPECIFIC ANTIGEN INCREASED |
| 5742248 | RED BLOOD CELL COUNT DECREASED |
| 5742248 | RESTLESSNESS |
| 5742248 | VOMITING |
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 |
|---|---|---|---|---|---|
| 5742248 | 1009923978 | 20080508 |