BECONASE Side Effects

6945106-8 | Ear Discomfort, Ill-defined Disorder, Product Quality Issue
on Jul 30, 2010 Female patient from UNITED STATES , 59 years of age, was diagnosed with ill-defined disorder, nasal inflammation and was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: ear discomfort, ill-defined disorder, product quality issue. Beconase dosage: 2spr Twice Per Day. During the same period patient was treated with FLONASE (2spr Per Day) (View Flonase Review and Flonase Label ), VERAMYST (1spr Per Day) (View Veramyst Review and Veramyst Label ).

6945105-6 | Migraine
Patient was taking Beconase (View Usage). Patient had the following side effects: migraine (What is migraine?) on Nov 09, 2009 from UNITED STATES Additional patient health information: Female patient , 59 years of age, . Beconase dosage: .

6945101-9 | Product Quality Issue
Adverse event was reported on Oct 26, 2009 by a Female patient taking Beconase (View Usage) (Dosage: ) . Location: UNITED STATES , 62 years of age, After Beconase was administered, patient had the following side effects: product quality issue. During the same period patient was treated with SINGULAIR (View Singulair Review and Singulair Label ), AZMACORT (View Azmacort Review and Azmacort Label ), SECTRAL (View Sectral Review and Sectral Label ), CORTISOL (View Cortisol Review and Cortisol Label ), NEXIUM (View Nexium Review and Nexium Label ), LIMBREL (View Limbrel Review and Limbrel Label ).

6721958-1 | Anosmia, Dysgeusia, Epistaxis, Nasal Odour
on May 06, 2010 Male patient from UNITED STATES , 51 years of age, was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: anosmia, dysgeusia, epistaxis, nasal odour. Beconase dosage: 2spr Twice Per Day. During the same period patient was treated with FLONASE (1spr Twice Per Day) (View Flonase Review and Flonase Label ), VERAMYST (1spr Twice Per Day) (View Veramyst Review and Veramyst Label ), ALBUTEROL SULATE (View Albuterol Sulate Review and Albuterol Sulate Label ), STEROID INHALED (View Steroid Inhaled Review and Steroid Inhaled Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), PROTONIX (View Protonix Review and Protonix Label ).


6439601-8 | Ageusia, Anosmia, Dyspnoea
on Nov 05, 2009 Female patient from AUSTRALIA , 65 years of age, was treated with Beconase (View Usage). Patient had the following side effects: ageusia, anosmia, dyspnoea. Beconase dosage: . During the same period patient was treated with PERIACTIN (View Periactin Review and Periactin Label ).

6349310-1 | Infertility, Spermatozoa Morphology Abnormal, Spermatozoa Progressive Motility Abnormal
Patient was taking Beconase (View Usage). After Beconase was administered, patient had the following side effects: infertility (What is infertility?), spermatozoa morphology abnormal, spermatozoa progressive motility abnormal on Sep 03, 2009 from AUSTRALIA Additional patient health information: Male patient , 42 years of age, . Beconase dosage: . During the same period patient was treated with ACIMAX (10mg Alternate Days) (View Acimax Review and Acimax Label ), PROPULSID (View Propulsid Review and Propulsid Label ).

6333345-9 | Product Quality Issue
Adverse event was reported on May 22, 2009 by a Female patient taking Beconase (View Usage) (Dosage: ) . Location: UNITED STATES , 62 years of age, Patient experienced the following unwanted or unexpected effects: product quality issue. During the same period patient was treated with SINGULAIR (View Singulair Review and Singulair Label ), AZMACORT (View Azmacort Review and Azmacort Label ), SECTRAL (View Sectral Review and Sectral Label ), CORTISOL (View Cortisol Review and Cortisol Label ), NEXIUM (View Nexium Review and Nexium Label ), LIMBREL (View Limbrel Review and Limbrel Label ).

6333343-5 | Application Site Erythema, Application Site Pruritus, Application Site Rash
on May 11, 2009 Female patient from UNITED STATES , 48 years of age, was diagnosed with application site reaction, pain (What is pain?) and was treated with Beconase (View Usage). Patient had the following side effects: application site erythema, application site pruritus, application site rash. Beconase dosage: . During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ).

6333342-3 | Dysgeusia, Oropharyngeal Pain, Product Quality Issue
on Jul 13, 2009 Female patient from UNITED STATES , 41 years of age, was diagnosed with sinus congestion and was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: dysgeusia, oropharyngeal pain, product quality issue. Beconase dosage: 2spr Per Day.

6333341-1 | Parosmia
Patient was taking Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: parosmia on Apr 09, 2009 from UNITED STATES Additional patient health information: Female patient , 61 years of age, . Beconase dosage: 1spr Twice Per Day. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ).

6333338-1 | Diplopia, Eye Movement Disorder, Oedema Peripheral, Product Quality Issue, Therapeutic Response Unexpected, Vision Blurred, Visual Impairment
Adverse event was reported on Mar 06, 2009 by a Male patient taking Beconase (View Usage) (Dosage: 2spr Twice Per Day) was diagnosed with epistaxis and. Location: UNITED STATES , 54 years of age, Patient had the following side effects: diplopia, eye movement disorder, oedema peripheral, product quality issue, therapeutic response unexpected, vision blurred, visual impairment. During the same period patient was treated with OXYCONTIN (View Oxycontin Review and Oxycontin Label ), MORPHINE (View Morphine Review and Morphine Label ), VALIUM (View Valium Review and Valium Label ), LEVOTHYROXINE (View Levothyroxine Review and Levothyroxine Label ), SINGULAIR (View Singulair Review and Singulair Label ), CLARINEX (View Clarinex Review and Clarinex Label ), FLOVENT (View Flovent Review and Flovent Label ).

6333337-X | Burning Sensation, Product Quality Issue
on Dec 16, 2008 Female patient from UNITED STATES , 83 years of age, was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: burning sensation, product quality issue. Beconase dosage: . During the same period patient was treated with CLARITIN (View Claritin Review and Claritin Label ), SALINE (View Saline Review and Saline Label ).

6333336-8 | Nasal Inflammation, Rhinalgia
on Sep 10, 2008 Female patient from UNITED STATES , 80 years of age, was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: nasal inflammation, rhinalgia. Beconase dosage: 84mcg Twice Per Day. During the same period patient was treated with DILTIAZEM (View Diltiazem Review and Diltiazem Label ), LIPITOR (View Lipitor Review and Lipitor Label ), ALUPENT (View Alupent Review and Alupent Label ), AZMACORT (View Azmacort Review and Azmacort Label ).

6332803-0 | Infertility
Patient was taking Beconase (View Usage). Patient had the following side effects: infertility (What is infertility?) on Aug 21, 2009 from AUSTRALIA Additional patient health information: Male patient , 42 years of age, . Beconase dosage: . During the same period patient was treated with ACIMAX (View Acimax Review and Acimax Label ), PROPULSID (View Propulsid Review and Propulsid Label ).

6203984-4 | Migraine
Adverse event was reported on May 19, 2009 by a Female patient taking Beconase (View Usage) (Dosage: 2app Twice Per Day) was diagnosed with asthma (What is asthma?), blood pressure (What is blood pressure?), pain (What is pain?) and. Location: FINLAND , 57 years of age, After Beconase was administered, patient had the following side effects: migraine (What is migraine?). During the same period patient was treated with SERETIDE (2app Three Times Per Day) (View Seretide Review and Seretide Label ), AMLODIPINE (10mg Per Day) (View Amlodipine Review and Amlodipine Label ), BURANA (View Burana Review and Burana Label ), PANACOD (View Panacod Review and Panacod Label ).

6071012-X | Cheilitis, Conjunctivitis, Eosinophilia, Erythema, Erythema Multiforme, Eye Disorder, Inflammation, Lymphopenia, Mouth Ulceration
on Jan 28, 2009 Female patient from FRANCE , 51 years of age, was diagnosed with skin lesion and was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: cheilitis, conjunctivitis, eosinophilia, erythema, erythema multiforme, eye disorder, inflammation, lymphopenia, mouth ulceration. Beconase dosage: . During the same period patient was treated with CELESTENE (1unit Per Day) (View Celestene Review and Celestene Label ), SOLUPRED (View Solupred Review and Solupred Label ), NAAXIA (View Naaxia Review and Naaxia Label ), ENOXOLONE (View Enoxolone Review and Enoxolone Label ). Patient was hospitalized.

6042916-9 | Ankle Fracture, Dyspnoea, Lower Respiratory Tract Infection, Malaise, Nasopharyngitis, Polymyalgia Rheumatica
on Jan 13, 2009 Female patient from UNITED KINGDOM , 59 years of age, was diagnosed with asthma (What is asthma?) and was treated with Beconase (View Usage). Patient had the following side effects: ankle fracture, dyspnoea, lower respiratory tract infection, malaise, nasopharyngitis, polymyalgia rheumatica (What is polymyalgia rheumatica?). Beconase dosage: . During the same period patient was treated with SERETIDE (3puff Twice Per Day) (View Seretide Review and Seretide Label ), VENTOLIN (100mcg As Required) (View Ventolin Review and Ventolin Label ), PREDNISOLONE (3mg Per Day) (View Prednisolone Review and Prednisolone Label ), LANSOPRAZOLE (30mg Per Day) (View Lansoprazole Review and Lansoprazole Label ). Patient was hospitalized.

5932782-1 | Lower Respiratory Tract Infection, Polymyalgia Rheumatica
Patient was taking Beconase (View Usage). After Beconase was administered, patient had the following side effects: lower respiratory tract infection, polymyalgia rheumatica (What is polymyalgia rheumatica?) on Oct 21, 2008 from UNITED KINGDOM Additional patient health information: Female patient , 59 years of age, was diagnosed with asthma (What is asthma?) and. Beconase dosage: . During the same period patient was treated with SERETIDE (2puff Twice Per Day) (View Seretide Review and Seretide Label ), VENTOLIN (100mcg As Required) (View Ventolin Review and Ventolin Label ).

5865275-0 | Agitation, Asthenia, Contusion, Influenza Like Illness, Tinnitus, Wheezing
Adverse event was reported on Jun 26, 2008 by a Male patient taking Beconase (View Usage) (Dosage: ) . Location: UNITED STATES , 64 years of age, Patient experienced the following unwanted or unexpected effects: agitation, asthenia, contusion, influenza like illness, tinnitus (What is tinnitus?), wheezing.

5865274-9 | Epistaxis
on Apr 21, 2008 Male patient from UNITED STATES , 67 years of age, was diagnosed with chronic sinusitis and was treated with Beconase (View Usage). Patient had the following side effects: epistaxis. Beconase dosage: . During the same period patient was treated with CLINDAMYCIN (View Clindamycin Review and Clindamycin Label ).

5865272-5 | Parosmia
on Apr 28, 2008 Male patient from UNITED STATES , 59 years of age, was diagnosed with sinus congestion and was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: parosmia. Beconase dosage: 1puff Twice Per Day.

5865268-3 | Bronchitis, Upper Respiratory Tract Infection
Patient was taking Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: bronchitis (What is bronchitis?), upper respiratory tract infection on Feb 01, 2008 from UNITED STATES Additional patient health information: Female patient , 61 years of age, . Beconase dosage: 2puff Per Day. During the same period patient was treated with FOSAMAX (View Fosamax Review and Fosamax Label ).

5865267-1 | Influenza Like Illness, Nasal Discomfort, Overdose
Adverse event was reported on Feb 12, 2008 by a Female patient taking Beconase (View Usage) (Dosage: ) was diagnosed with multiple allergies and. Location: UNITED STATES , 63 years of age, Patient had the following side effects: influenza like illness, nasal discomfort, overdose. During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ).

5865265-8 | Headache
on Sep 12, 2007 Female patient from UNITED STATES , 56 years of age, was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: headache (What is headache?). Beconase dosage: 1spr Twice Per Day. During the same period patient was treated with FLONASE (4spr Per Day) (View Flonase Review and Flonase Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), AVONEX (View Avonex Review and Avonex Label ), DETROL (View Detrol Review and Detrol Label ), ENTOCORT EC (View Entocort Ec Review and Entocort Ec Label ), ACIPHEX (View Aciphex Review and Aciphex Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ).

5865262-2 | Hypersensitivity, Sinus Headache
on Aug 15, 2007 Female patient from UNITED STATES , 48 years of age, was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: hypersensitivity, sinus headache. Beconase dosage: 2spr Twice Per Day.

5757055-1 | Blood Pressure Increased, Dizziness, Headache, Hypertension, Tinnitus
Patient was taking Beconase (View Usage). Patient had the following side effects: blood pressure increased, dizziness (What is dizziness?), headache (What is headache?), hypertension, tinnitus (What is tinnitus?) on May 29, 2008 from FRANCE Additional patient health information: Female patient , 42 years of age, weighting 154.3 lb, . Beconase dosage: 2puff Twice Per Day.

5721177-1 | Blood Pressure Increased, Headache, Hypertension
Adverse event was reported on Apr 24, 2008 by a Female patient taking Beconase (View Usage) (Dosage: 2puff Twice Per Day) . Location: FRANCE , 42 years of age, After Beconase was administered, patient had the following side effects: blood pressure increased, headache (What is headache?), hypertension.

5592983-1 | Dyspnoea, Influenza Like Illness, Lymphadenopathy, Nasal Congestion, Pharyngeal Oedema, Pharyngolaryngeal Pain, Sinusitis, Wheezing
on Jan 14, 2008 Female patient from UNITED STATES , 19 years of age, weighting 165.3 lb, was diagnosed with prophylaxis, seasonal allergy and was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, influenza like illness, lymphadenopathy, nasal congestion, pharyngeal oedema, pharyngolaryngeal pain, sinusitis (What is sinusitis?), wheezing. Beconase dosage: 1 Spray Into Each Nostril Once Per Day Nasal (duration: Used Once).

5566785-6 | Dysgraphia, Tremor
on Dec 18, 2007 Male patient from UNITED STATES , 40 years of age, was treated with Beconase (View Usage). Patient had the following side effects: dysgraphia, tremor. Beconase dosage: 1spr Twice Per Day. During the same period patient was treated with DEPAKOTE (View Depakote Review and Depakote Label ), KLONOPIN (View Klonopin Review and Klonopin Label ), SEROQUEL (View Seroquel Review and Seroquel Label ).

5429542-7 | Mental Impairment
Patient was taking Beconase (View Usage). After Beconase was administered, patient had the following side effects: mental impairment on Jun 29, 2007 from UNITED STATES Additional patient health information: Female patient , 77 years of age, . Beconase dosage: 42mcg Twice Per Day. During the same period patient was treated with LEVOXYL (View Levoxyl Review and Levoxyl Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), CALCIUM (View Calcium Review and Calcium Label ), M.V.I. (View M.v.i. Review and M.v.i. Label ).

5429540-3 | Haemoptysis, Nasal Discomfort
Adverse event was reported on Jun 13, 2007 by a Male patient taking Beconase (View Usage) (Dosage: 336mcg Three Times Per Day) . Location: UNITED STATES , 54 years of age, Patient experienced the following unwanted or unexpected effects: haemoptysis, nasal discomfort. During the same period patient was treated with OXYCONTIN (View Oxycontin Review and Oxycontin Label ), VALIUM (View Valium Review and Valium Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ).

5429539-7 | Intraocular Pressure Increased
on May 08, 2007 Female patient from UNITED STATES , 81 years of age, was treated with Beconase (View Usage). Patient had the following side effects: intraocular pressure increased. Beconase dosage: 2spr Per Day. During the same period patient was treated with HYZAAR (View Hyzaar Review and Hyzaar Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), CHOLESTYRAMINE (View Cholestyramine Review and Cholestyramine Label ).

5429534-8 | Ageusia, Anosmia
on Feb 15, 2007 Female patient from UNITED STATES , 59 years of age, was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: ageusia, anosmia. Beconase dosage: 1spr Twice Per Day. During the same period patient was treated with ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), ASTRAGALUS (View Astragalus Review and Astragalus Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ).

5429533-6 | Aphonia, Cough
Patient was taking Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: aphonia, cough on Apr 11, 2007 from UNITED STATES Additional patient health information: Female patient , 78 years of age, . Beconase dosage: 2puff Variable Dose.

5429527-0 | Dry Throat, Incorrect Dose Administered, Laryngitis, Pharyngolaryngeal Pain, Speech Disorder
Adverse event was reported on Nov 13, 2006 by a Female patient taking Beconase (View Usage) (Dosage: ) . Location: UNITED STATES , 69 years of age, Patient had the following side effects: dry throat, incorrect dose administered, laryngitis, pharyngolaryngeal pain, speech disorder. During the same period patient was treated with REQUIP (View Requip Review and Requip Label ), XALATAN (View Xalatan Review and Xalatan Label ), ZESTRIL (View Zestril Review and Zestril Label ), ZIAC (View Ziac Review and Ziac Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ).

5339511-3 | Gait Disturbance, Lower Limb Deformity, Osteonecrosis, Unequal Limb Length
on May 08, 2007 Female patient from UNITED KINGDOM , 47 years of age, was diagnosed with asthma (What is asthma?) and was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: gait disturbance, lower limb deformity, osteonecrosis (What is osteonecrosis?), unequal limb length. Beconase dosage: 2 Puff (s) / Twice Per Day/ Inhaled.

5280310-9 | Hepatic Neoplasm Malignant, Ill-defined Disorder, Oesophageal Adenocarcinoma, Oesophageal Cancer Metastatic
on Mar 22, 2007 Male patient from UNITED KINGDOM , 74 years of age, was diagnosed with asthma (What is asthma?) and was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: hepatic neoplasm malignant, ill-defined disorder, oesophageal adenocarcinoma, oesophageal cancer metastatic. Beconase dosage: . During the same period patient was treated with BECOTIDE (View Becotide Review and Becotide Label ).

5145416-3 | Blood Corticotrophin Decreased, Blood Cortisol Decreased, Chest Pain, Cushing's Syndrome, Ventricular Dysfunction
Patient was taking Beconase (View Usage). Patient had the following side effects: blood corticotrophin decreased, blood cortisol decreased, chest pain (What is chest pain?), cushing's syndrome, ventricular dysfunction on Oct 23, 2006 from UNITED KINGDOM Additional patient health information: Male patient , 53 years of age, was diagnosed with asthma (What is asthma?) and. Beconase dosage: 200 Mcg/twice Per Day/ Inhaled. During the same period patient was treated with STEROID (View Steroid Review and Steroid Label ), ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ).

5091340-4 | Nasal Discomfort, Pruritus
Adverse event was reported on Mar 23, 2006 by a Female patient taking Beconase (View Usage) (Dosage: 2spr Per Day) was diagnosed with nasal congestion and. Location: UNITED STATES , 73 years of age, After Beconase was administered, patient had the following side effects: nasal discomfort, pruritus.

5091339-8 | Rhinalgia
on Feb 28, 2006 Male patient from UNITED STATES , 66 years of age, was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: rhinalgia. Beconase dosage: 2spr Per Day. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), GLIPIZIDE (View Glipizide Review and Glipizide Label ), NEXIUM (View Nexium Review and Nexium Label ), LIPITOR (View Lipitor Review and Lipitor Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), COREG (View Coreg Review and Coreg Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ).

5091337-4 | Dysgeusia, Headache
on Feb 08, 2006 Female patient from UNITED STATES , 81 years of age, was treated with Beconase (View Usage). Patient had the following side effects: dysgeusia, headache (What is headache?). Beconase dosage: 1spr Twice Per Day. During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), NEXIUM (View Nexium Review and Nexium Label ).

5091335-0 | Nasal Discomfort, Sinusitis, Sneezing
Patient was taking Beconase (View Usage). After Beconase was administered, patient had the following side effects: nasal discomfort, sinusitis (What is sinusitis?), sneezing on Jan 30, 2006 from UNITED STATES Additional patient health information: Female patient , 43 years of age, . Beconase dosage: 2spr Per Day. During the same period patient was treated with ANTIBIOTIC (View Antibiotic Review and Antibiotic Label ).

5091334-9 | Nasal Discomfort, Sinusitis, Sneezing
Adverse event was reported on Jan 30, 2006 by a Female patient taking Beconase (View Usage) (Dosage: 2spr Per Day) . Location: UNITED STATES , 68 years of age, Patient experienced the following unwanted or unexpected effects: nasal discomfort, sinusitis (What is sinusitis?), sneezing. During the same period patient was treated with ANTIBIOTIC (View Antibiotic Review and Antibiotic Label ).

5091333-7 | Nasal Dryness, Nasal Odour
on Jan 19, 2006 Female patient from UNITED STATES , 46 years of age, was treated with Beconase (View Usage). Patient had the following side effects: nasal dryness, nasal odour. Beconase dosage: 84mcg Twice Per Day. During the same period patient was treated with CLARINEX (View Clarinex Review and Clarinex Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

5091331-3 | Sinus Disorder
on Jan 06, 2006 Male patient from UNITED STATES , 57 years of age, was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: sinus disorder. Beconase dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), NEXIUM (View Nexium Review and Nexium Label ).

5091328-3 | Epistaxis
Patient was taking Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: epistaxis on Aug 23, 2005 from UNITED STATES Additional patient health information: Female patient , 71 years of age, . Beconase dosage: 1spr Twice Per Day.

5034189-0 | Collapse Of Lung
Adverse event was reported on Jun 22, 2006 by a Male patient taking Beconase (View Usage) (Dosage: 42mcg Per Day) . Location: UNITED STATES , 58 years of age, Patient had the following side effects: collapse of lung. Patient was hospitalized.

4980431-1 | Dyspnoea, Muscular Weakness, Vertigo
on Apr 12, 2006 Female patient from AUSTRALIA , 83 years of age, was diagnosed with sinus disorder and was treated with Beconase (View Usage). After Beconase was administered, patient had the following side effects: dyspnoea, muscular weakness, vertigo. Beconase dosage: 2puff Twice Per Day. During the same period patient was treated with SERETIDE (View Seretide Review and Seretide Label ), EZETROL (View Ezetrol Review and Ezetrol Label ). Patient was hospitalized.

4753617-9 | Parosmia
on May 12, 2005 Male patient from UNITED STATES , 62 years of age, was treated with Beconase (View Usage). Patient experienced the following unwanted or unexpected effects: parosmia. Beconase dosage: 2spr Twice Per Day.

4753615-5 | Nasal Congestion
Patient was taking Beconase (View Usage). Patient had the following side effects: nasal congestion on Mar 15, 2005 from UNITED STATES Additional patient health information: Male patient , 60 years of age, . Beconase dosage: 2puff Twice Per Day. During the same period patient was treated with CLARITIN (View Claritin Review and Claritin Label ), NASALCROM (View Nasalcrom Review and Nasalcrom Label ).