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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8248782 | 8201937 | F | 8248782-5 | 20110722 | 20120322 | 20120331 | EXP | PHHO2011US12831 | NOVARTIS PHARMACEUTICAL CORPORATION | 79 | YR | F | Y | 70.4 | KG | 20120328 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8248782 | 1019282875 | C | FOSAMAX | 1 | ORAL | 35 MG, QW | |||||
8248782 | 1019282876 | C | METOPROLOL SUCCINATE | 1 | ORAL | 12.4 MG, QD | |||||
8248782 | 1019282868 | PS | EXELON | 1 | TRANSDERMAL | 9 MG/5CM2 | 022083 | ||||
8248782 | 1019282870 | SS | EXELON | 1 | UNK | 022083 | |||||
8248782 | 1019282878 | C | ASPIRIN | 1 | ORAL | 81 MG, QD | |||||
8248782 | 1019282871 | C | NAMENDA | 1 | ORAL | 10 MG, BID | |||||
8248782 | 1019282874 | C | AMLODIPINE BESYLATE AND BENAZEPRIL HCL | 1 | ORAL | 540 MG, QD | |||||
8248782 | 1019282881 | C | CALCIUM CARBONATE | 1 | ORAL | 600400 MG, QD | |||||
8248782 | 1019282869 | SS | BLINDED NO TREATMENT RECEIVED | 2 | TRANSDERMAL | 9 MG/5CM2 | 022083 | ||||
8248782 | 1019282873 | C | RISPERDAL | 1 | ORAL | 0.5 MG, PRN | |||||
8248782 | 1019282877 | C | MIRALAX | 1 | ORAL | 17 G, QD | |||||
8248782 | 1019282872 | C | CITALOPRAM HYDROBROMIDE | 1 | ORAL | 20 MG, QD | |||||
8248782 | 1019282880 | C | DOCUSATE SODIUM | 2 | ORAL | 100 MG, TID | |||||
8248782 | 1019282882 | C | VITAMIN D | 1 | |||||||
8248782 | 1019282879 | C | ZOCOR | 1 | ORAL | 40 MG, QD |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8248782 | 1019282875 | OSTEOPOROSIS |
8248782 | 1019282876 | HYPERTENSION |
8248782 | 1019282868 | DEMENTIA ALZHEIMER'S TYPE |
8248782 | 1019282870 | DEMENTIA ALZHEIMER'S TYPE |
8248782 | 1019282878 | PROPHYLAXIS |
8248782 | 1019282871 | DEMENTIA ALZHEIMER'S TYPE |
8248782 | 1019282874 | HYPERTENSION |
8248782 | 1019282881 | SUPPLEMENTATION THERAPY |
8248782 | 1019282869 | DEMENTIA ALZHEIMER'S TYPE |
8248782 | 1019282873 | ANXIETY |
8248782 | 1019282877 | CONSTIPATION |
8248782 | 1019282872 | DEPRESSION |
8248782 | 1019282880 | CONSTIPATION |
8248782 | 1019282879 | HYPERCHOLESTEROLAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
8248782 | HO |
Reactions reported
Event ID | PT |
---|---|
8248782 | DEHYDRATION |
8248782 | MENTAL STATUS CHANGES |
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 |
---|---|---|---|---|---|
8248782 | 1019282875 | 20101001 | |||
8248782 | 1019282876 | 20110516 | |||
8248782 | 1019282868 | 20110621 | 20110722 | 32 | DAY |
8248782 | 1019282878 | 20110414 | |||
8248782 | 1019282871 | 20070101 | |||
8248782 | 1019282874 | 20100923 | |||
8248782 | 1019282881 | 20101004 | |||
8248782 | 1019282869 | 20110621 | 20110722 | 32 | DAY |
8248782 | 1019282873 | 20100921 | |||
8248782 | 1019282877 | 20101007 | |||
8248782 | 1019282872 | 20100101 | |||
8248782 | 1019282880 | 20110504 | |||
8248782 | 1019282879 | 20110223 |