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Index of reports
> Cases resulting in hospitalization (19)
Below is the selection of adverse event reports related to Pulmicort (Budesonide Inhalation) that includes cases resulting in hospitalization.
Adverse event in 86 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a consumer/non-health professional from United States on 2007-10-01
Patient: 86 year old female, weighing 47.7 kg (104.9 pounds)
Adverse reactions / side effects: Rash Pustular, Hyponatraemia, Nasal Septum Ulceration
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Rhinocort
Xopenex
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2006-12-01
End date: 2007-04-01
Xopenex HFA Inhalation Aerosol
Administration route: Oral
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2007-04-01
Spiriva
End date: 2007-07-01
Other drugs received by patient: Oxygen; Lisinopril; Levothyroxine Sodium; Sodium Chloride
Adverse event in 35 year old male receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-31
Patient: 35 year old male
Adverse reactions / side effects: Asthma, Pharyngeal Oedema, Tongue Oedema, Oedema Mouth, Paraesthesia
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Pulmicort (Budesonide Inhalation)
Other drugs received by patient: Becodisks
Adverse event in 68 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a physician from Japan on 2007-07-23
Patient: 68 year old female, weighing 64.0 kg (140.8 pounds)
Adverse reactions / side effects: Malaise, Pyrexia, Cold Sweat
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Indication: Asthma
Start date: 2007-05-30
End date: 2007-06-13
Feron
Dosage: 300 x 104 u/week
Indication: Hepatitis C
Start date: 2006-10-05
End date: 2006-11-22
Feron
Dosage: 300 x 104 u/week
Indication: Hepatic Cirrhosis
Start date: 2006-10-05
End date: 2006-11-22
Feron
Dosage: 300 x 104 u/week
Start date: 2007-03-05
End date: 2007-05-30
Feron
Dosage: 300 x 104 u/week
Start date: 2007-03-05
End date: 2007-05-30
Feron
Dosage: 300 x 104 u/week
Start date: 2007-06-13
End date: 2007-06-13
Feron
Dosage: 300 x 104 u/week
Start date: 2007-06-13
End date: 2007-06-13
Other drugs received by patient: Onon; Codeine Phosphate; Aminoleban; Aminoleban; Aminoleban; Lasix; Lasix; Famotidine; Loxonin; Candesartan Cilexetil; Magnesium Oxide; Urso 250; Urso 250
Adverse event in 68 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a physician from Japan on 2007-07-13
Patient: 68 year old female, weighing 64.0 kg (140.8 pounds)
Adverse reactions / side effects: Malaise, Pyrexia, Cold Sweat
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Indication: Asthma
Start date: 2007-05-30
End date: 2007-06-13
Interferon Beta
Indication: Hepatitis C
Start date: 2006-10-05
End date: 2006-11-22
Interferon Beta
Indication: Hepatic Cirrhosis
Start date: 2006-10-05
End date: 2006-11-22
Interferon Beta
Start date: 2007-03-01
End date: 2007-06-14
Interferon Beta
Start date: 2007-03-01
End date: 2007-06-14
Other drugs received by patient: Onon; Codeine Phosphate; Aminoleban; Aminoleban; Lasix; Lasix; Gaster D; Loxonin; Blopress; Magnesium Oxide; Urso 250; Urso 250
Adverse event in 48 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from France on 2007-07-02
Patient: 48 year old female, weighing 71.0 kg (156.2 pounds)
Adverse reactions / side effects: Neutropenia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Symbicort
Omeprazole
Administration route: Oral
Izilox
Administration route: Oral
Indication: Pneumonia
Start date: 2007-05-03
End date: 2007-05-16
Imovane
Administration route: Oral
Indication: Sleep Disorder
Start date: 2007-05-04
End date: 2007-05-25
Cortancyl
Administration route: Oral
Indication: Polyarthritis
Tramadol HCL
Administration route: Oral
Spiriva
Adverse event in 68 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a physician from Japan on 2007-06-29
Patient: 68 year old female
Adverse reactions / side effects: Malaise, Pyrexia, Cold Sweat
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Indication: Asthma
Start date: 2007-05-30
End date: 2007-06-14
Interferon Beta
Indication: Hepatitis C
Start date: 2007-03-05
Interferon Beta
Indication: Hepatic Cirrhosis
Start date: 2007-03-05
Other drugs received by patient: Aminoleban; Lasix; Gaster D; Loxonin; Blopress; Codeine Phosphate; Magnesium Oxide; Pranlukast Hydrate
Adverse event in 69 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-27
Patient: 69 year old female
Adverse reactions / side effects: Klebsiella Infection, Arthritis Bacterial, Condition Aggravated, Skin Necrosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Cortancyl
Administration route: Oral
Arava
Administration route: Oral
End date: 2007-04-18
Humira
End date: 2007-02-15
Adverse event in 30 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a individual with unspecified qualification from Netherlands on 2007-05-15
Patient: 30 year old female, weighing 82.0 kg (180.4 pounds)
Adverse reactions / side effects: Cushing's Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort (Budesonide Inhalation)
Adverse event in 77 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from Spain on 2007-05-01
Patient: 77 year old female
Adverse reactions / side effects: Toxic Epidermal Necrolysis
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Adiro
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Zinnat 125 MG
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-01
Omeprazole
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-01
Seguril
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Nsaid
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Feldene
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Manidon
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Fosamax
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Deanxit 10 / 0.5 MG (Flupentixol)
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-01
Spiriva
Indication: Drug USE FOR Unknown Indication
Pulmicort
Indication: Drug USE FOR Unknown Indication
Flumil
Indication: Drug USE FOR Unknown Indication
Ferrum
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 43 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-11
Patient: 43 year old female
Adverse reactions / side effects: Eyelid Oedema, Face Oedema, Urticaria, Erythema
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort (Budesonide Inhalation)
Other drugs received by patient: Celestene; Ketek
Adverse event in receiving Pulmicort (Budesonide Inhalation)
Reported by a pharmacist from France on 2007-04-03
Patient:
Adverse reactions / side effects: Dysuria, Urinary Retention
Adverse event resulted in: hospitalization
Suspect drug(s):
Intal
Dosage: 4 u, qd
Indication: Asthma
Start date: 2006-12-15
End date: 2006-12-30
Pulmicort
Other drugs received by patient: Ventoline / 00139501 /
Adverse event in 79 year old male receiving Pulmicort (Budesonide Inhalation)
Reported by a consumer/non-health professional from Japan on 2007-03-22
Patient: 79 year old male
Adverse reactions / side effects: Extrasystoles
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort (Budesonide Inhalation)
Other drugs received by patient: Evamyl
Adverse event in female receiving Pulmicort (Budesonide Inhalation)
Reported by a physician from Sweden on 2007-03-07
Patient: female
Adverse reactions / side effects: Vocal Cord Thickening, Tracheal Neoplasm
Adverse event resulted in: hospitalization
Suspect drug(s):
Symbicort
Dosage: 320/9 ug/inhalation, bid
Indication: Asthma
Start date: 2005-10-25
End date: 2006-11-16
Pulmicort
Indication: Asthma
Start date: 2005-10-25
End date: 2006-11-16
Terbutaline Turbuhaler
Indication: Asthma
Start date: 2005-10-25
End date: 2006-11-16
Other drugs received by patient: Salures-K; Zanidip; Artrox; Reductil; Flutide Nasal; Orudis; Claritin; Orudis Retard; Orudis Retard
Adverse event in female receiving Pulmicort (Budesonide Inhalation)
Reported by a consumer/non-health professional from United States on 2007-03-07
Patient: female
Adverse reactions / side effects: Chronic Obstructive Pulmonary Disease
Adverse event resulted in: hospitalization
Suspect drug(s):
Spiriva
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2005-12-01
Pulmicort
Indication: Chronic Obstructive Pulmonary Disease
Start date: 2006-02-01
Adverse event in 71 year old male receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from France on 2007-02-23
Patient: 71 year old male, weighing 86.0 kg (189.2 pounds)
Adverse reactions / side effects: Anaemia Haemolytic Autoimmune, Haemolytic Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Tahor
Administration route: Oral
Indication: Hypercholesterolaemia
Paracetamol
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Pulmicort
Administration route: Oral
Indication: Asthma
Cotareg
Dosage: text:160
Administration route: Oral
Indication: Hypertension
Adverse event in 39 year old male receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from France on 2007-02-20
Patient: 39 year old male
Adverse reactions / side effects: Anxiety, Abnormal Behaviour, Paraesthesia
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Start date: 2007-01-04
End date: 2007-01-07
Tussidane
Administration route: Oral
Start date: 2007-01-04
End date: 2007-01-07
Mononaxy
Administration route: Oral
Start date: 2007-01-04
End date: 2007-01-07
Adverse event in 16 year old female receiving Pulmicort (Budesonide Inhalation)
Reported by a physician from United States on 2007-01-30
Patient: 16 year old female, weighing 45.4 kg (99.9 pounds)
Adverse reactions / side effects: Dizziness, Depression, Suicidal Ideation
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Indication: Asthma
Start date: 2006-10-14
End date: 2006-10-29
Pulmicort
Start date: 2006-10-30
End date: 2006-11-26
Pulmicort
Start date: 2006-12-01
End date: 2006-12-09
Other drugs received by patient: Methylprednisolone 16mg TAB; Loratadine; Loratadine; Albuterol; Albuterol; Albuterol; Singulair
Adverse event in 71 year old male receiving Pulmicort (Budesonide Inhalation)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-25
Patient: 71 year old male, weighing 86.0 kg (189.2 pounds)
Adverse reactions / side effects: Haemolytic Anaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Indication: Asthma
Doliprane
Administration route: Oral
Atorvastatin Calcium
Administration route: Oral
Indication: Hypercholesterolaemia
Valsartan and Hydrochlorothiazide
Administration route: Oral
Indication: Hypertension
Adverse event in male receiving Pulmicort (Budesonide Inhalation)
Reported by a consumer/non-health professional from United States on 2007-01-17
Patient: male, weighing 5.4 kg (11.9 pounds)
Adverse reactions / side effects: Femur Fracture, Constipation, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Pulmicort
Indication: Tracheal Disorder
Start date: 2006-11-01
Xopenex
Dosage: 0.63 mg / 3 ml prn
Indication: Tracheal Disorder
Start date: 2006-11-01
End date: 2006-12-01
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