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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7235936 | 7276183 | F | 7235936-X | 20110111 | 20110120 | EXP | A0843829A | GLAXOSMITHKLINE | YR | F | Y | 20110120 | CN | CUBA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7235936 | 1015564255 | PS | FLUTICASONE PROPIONATE/SALMETEROL | 1 | RESPIRATORY (INHALATION) | 021077 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
7235936 | OT |
Reactions reported
Event ID | PT |
---|---|
7235936 | LUNG DISORDER |
7235936 | NON-CARDIAC CHEST PAIN |
7235936 | DYSPNOEA |
7235936 | RENAL PAIN |
7235936 | NAUSEA |
7235936 | DIZZINESS |
7235936 | MALAISE |
7235936 | FLATULENCE |
7235936 | IRON DEFICIENCY ANAEMIA |
7235936 | ALOPECIA |
7235936 | MOUTH BREATHING |
7235936 | ARTHRALGIA |
7235936 | RESPIRATORY DISORDER |
7235936 | DISCOMFORT |
7235936 | DRY EYE |
7235936 | SLEEP DISORDER |
7235936 | ABDOMINAL PAIN UPPER |
7235936 | NASAL DISCOMFORT |
7235936 | HEADACHE |
7235936 | HYPERSENSITIVITY |
7235936 | ASTHMA |
7235936 | DRUG HYPERSENSITIVITY |
7235936 | GASTRITIS |
7235936 | INITIAL INSOMNIA |
7235936 | DISABILITY |
7235936 | WHEEZING |
7235936 | BONE PAIN |
7235936 | AMNESIA |
7235936 | MUSCLE SPASMS |
7235936 | OXYGEN CONSUMPTION INCREASED |
7235936 | PNEUMONITIS |
7235936 | EYE PAIN |
7235936 | CHOKING |
7235936 | RHINORRHOEA |
7235936 | PARAESTHESIA |
7235936 | SJOGREN'S SYNDROME |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |