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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4959781 | 6013849 | I | 4959781-0 | 20050829 | 20051128 | 20060331 | EXP | NL-BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.-2006-NL-00079NL | BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. | Y | 20060331 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4959781 | 1007117947 | PS | ATROVENT | 1 | 4-6DD1 | 19085 | |||||
| 4959781 | 1007117948 | C | LISINOPRIL | 1 | |||||||
| 4959781 | 1007117949 | C | FORMOTEROL | 2 | 12UG/DO 2DD1 | ||||||
| 4959781 | 1007117950 | C | HYDROCHLOROTHIAZIDE | 1 | |||||||
| 4959781 | 1007117951 | C | ACETYLSALICYLIC ACID SRT | 1 | |||||||
| 4959781 | 1007117952 | C | TEMAZEPAM | 1 | PRN | ||||||
| 4959781 | 1007117953 | C | FENTANYL | 1 | |||||||
| 4959781 | 1007117954 | C | ACETYLCYSTEINE | 1 | |||||||
| 4959781 | 1007117955 | C | PREDNISOLONE | 1 | |||||||
| 4959781 | 1007117956 | C | COTRIM | 1 | STRENGTH: 160/800MG | ||||||
| 4959781 | 1007117957 | C | CODEINE | 2 | PRN |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4959781 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4959781 | BLOOD PRESSURE INCREASED |
| 4959781 | CAROTID ARTERY STENOSIS |
| 4959781 | CEREBRAL INFARCTION |
| 4959781 | CEREBROVASCULAR ACCIDENT |
| 4959781 | DYSPHASIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |