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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7790822 | 8164729 | I | 7790822-1 | 20110921 | 20110930 | EXP | US-ASTRAZENECA-2007UW16054 | AZPRODUW00 | 43 | YR | F | Y | 77.1 | KG | 20110930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7790822 | 1017683792 | C | NORTRIPTYLINE HCL | 1 | |||||||
7790822 | 1017683793 | C | BLOOD PRESSURE MEDICATION | 2 | |||||||
7790822 | 1017683786 | SS | SEROQUEL | 1 | ORAL | 020639 | |||||
7790822 | 1017683789 | C | CYMBALTA | 1 | |||||||
7790822 | 1017683785 | PS | SEROQUEL | 1 | ORAL | 020639 | |||||
7790822 | 1017683787 | SS | SEROQUEL | 1 | ORAL | 020639 | |||||
7790822 | 1017683788 | SS | SEROQUEL | 1 | ORAL | 020639 | |||||
7790822 | 1017683790 | C | PREMARIN | 1 | |||||||
7790822 | 1017683791 | C | LOPRESSOR | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7790822 | 1017683786 | DEPRESSION |
7790822 | 1017683785 | BIPOLAR DISORDER |
Outcome of event
Event ID | OUTC COD |
---|---|
7790822 | OT |
Reactions reported
Event ID | PT |
---|---|
7790822 | HYPERHIDROSIS |
7790822 | CARDIAC DISORDER |
7790822 | MYOCARDIAL INFARCTION |
7790822 | ILL-DEFINED DISORDER |
7790822 | NAUSEA |
7790822 | DRY MOUTH |
7790822 | DRUG INEFFECTIVE |
7790822 | WEIGHT INCREASED |
7790822 | DEPRESSION |
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 |
---|---|---|---|---|---|
7790822 | 1017683786 | 20061001 | |||
7790822 | 1017683785 | 20061001 |