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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7023323 | 7173618 | F | 7023323-9 | 20080101 | 20100816 | 20100930 | EXP | US-BAXTER-2009BH017010 | BAXTER | 49 | YR | F | Y | 58 | KG | 20100930 | LW | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7023323 | 1014813744 | PS | HEPARIN SODIUM INJECTION | 1 | UNKNOWN | UNKNOWN | |||||
| 7023323 | 1014813745 | SS | HEPARIN SODIUM INJECTION | 1 | UNKNOWN | UNKNOWN | |||||
| 7023323 | 1014813746 | SS | HEPARIN SODIUM INJECTION | 1 | UNKNOWN | UNKNOWN | |||||
| 7023323 | 1014813747 | C | ACETAZOLAMIDE | 1 | UNKNOWN | ||||||
| 7023323 | 1014813748 | C | ASPIRIN | 1 | UNKNOWN | ||||||
| 7023323 | 1014813749 | C | VITAMIN D3 | 2 | ORAL | ||||||
| 7023323 | 1014813750 | C | COLACE | 2 | UNKNOWN | ||||||
| 7023323 | 1014813751 | C | FIORICET | 1 | ORAL | ||||||
| 7023323 | 1014813752 | C | FOSAMAX | 1 | UNKNOWN | ||||||
| 7023323 | 1014813753 | C | LEVETIRACETAM | 1 | UNKNOWN | ||||||
| 7023323 | 1014813754 | C | SULFAMETHOXAZOLE | 1 | ORAL | ||||||
| 7023323 | 1014813755 | C | DIAMOX SODIUM | 2 | ORAL | ||||||
| 7023323 | 1014813756 | C | KEPPRA | 1 | ORAL | ||||||
| 7023323 | 1014813757 | C | ASPIRIN | 1 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7023323 | 1014813744 | INTRACRANIAL ANEURYSM |
| 7023323 | 1014813747 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813748 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813749 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813750 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813751 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813752 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813753 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813754 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813755 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813756 | PRODUCT USED FOR UNKNOWN INDICATION |
| 7023323 | 1014813757 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7023323 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7023323 | ABDOMINAL PAIN |
| 7023323 | ASTHENIA |
| 7023323 | DECREASED APPETITE |
| 7023323 | HYPOTENSION |
| 7023323 | LETHARGY |
| 7023323 | MENTAL STATUS CHANGES |
| 7023323 | NAUSEA |
| 7023323 | SUBARACHNOID HAEMORRHAGE |
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 |
|---|---|---|---|---|---|
| 7023323 | 1014813745 | 20080129 | 20080130 | ||
| 7023323 | 1014813746 | 20080202 | 20080208 |