OMNARIS Side Effects

6970378-3 | Arthralgia, Dyspepsia, Headache, Hepatic Enzyme Increased, Idiopathic Thrombocytopenic Purpura, Musculoskeletal Stiffness, Myalgia, Pain, Pyrexia
on Aug 23, 2010 Female patient from UNITED STATES , 40 years of age, weighting 140.0 lb, was diagnosed with rhinitis allergic, dermatitis, lichen planus and was treated with Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, dyspepsia, headache (What is headache?), hepatic enzyme increased, idiopathic thrombocytopenic purpura, musculoskeletal stiffness, myalgia, pain (What is pain?), pyrexia. Omnaris dosage: 200 Ug; Qd; Nasal. During the same period patient was treated with MINOCIN (100 Mg; Qd; Oral, 0 Mg; Qd; Oral) (View Minocin Review and Minocin Label ), SYMBICORT (View Symbicort Review and Symbicort Label ).

6929685-2 | Dizziness, Hypertensive Crisis, Hypoaesthesia, Syncope, Visual Impairment
Patient was taking Omnaris (View Usage). Patient had the following side effects: dizziness (What is dizziness?), hypertensive crisis, hypoaesthesia, syncope, visual impairment on Jul 29, 2010 from GERMANY Additional patient health information: Female patient , 54 years of age, weighting 136.7 lb, was diagnosed with rhinitis allergic and. Omnaris dosage: 200 Ug; Qd; Nasal. During the same period patient was treated with CENTRUM (View Centrum Review and Centrum Label ), CALCIUM (View Calcium Review and Calcium Label ), FERROUS SULFATE (View Ferrous Sulfate Review and Ferrous Sulfate Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), LORAX (View Lorax Review and Lorax Label ).

6884974-5 | Arthralgia, Dyspepsia, Headache, Hepatic Enzyme Increased, Joint Stiffness, Musculoskeletal Stiffness, Pain, Pyrexia, Rash Pustular
Adverse event was reported on Jul 13, 2010 by a Female patient taking Omnaris (View Usage) (Dosage: 200 Ug; Qd; Nasal) was diagnosed with rhinitis allergic, dermatitis, lichen planus and. Location: UNITED STATES , 40 years of age, weighting 140.0 lb, After Omnaris was administered, patient had the following side effects: arthralgia, dyspepsia, headache (What is headache?), hepatic enzyme increased, joint stiffness, musculoskeletal stiffness, pain (What is pain?), pyrexia, rash pustular. During the same period patient was treated with MINOCIN (100 Mg; Qd; Oral 200 Mg; Qd; Oral) (View Minocin Review and Minocin Label ), SYMBICORT (View Symbicort Review and Symbicort Label ).

6883812-4 | Cataract, Condition Aggravated
on Jul 13, 2010 Female patient from GERMANY , 50 years of age, was diagnosed with rhinitis allergic and was treated with Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: cataract (What is cataract?), condition aggravated. Omnaris dosage: Nasal. During the same period patient was treated with BETAMETHASONE (View Betamethasone Review and Betamethasone Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).


6862496-5 | Cataract
on Jul 01, 2010 Female patient from GERMANY , 50 years of age, was diagnosed with rhinitis allergic and was treated with Omnaris (View Usage). Patient had the following side effects: cataract (What is cataract?). Omnaris dosage: Nasal.

6860908-4 | Arthralgia, Dyspepsia, Hepatic Enzyme Increased, Meningitis Viral, Pain, Rash Pustular, Serum Sickness-like Reaction, White Blood Cell Count Decreased
Patient was taking Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: arthralgia, dyspepsia, hepatic enzyme increased, meningitis viral, pain (What is pain?), rash pustular, serum sickness-like reaction, white blood cell count decreased on Jul 03, 2010 from UNITED STATES Additional patient health information: Female patient , 40 years of age, weighting 140.0 lb, was diagnosed with rhinitis allergic, lichen planus and. Omnaris dosage: 200ug;qd;nasal. During the same period patient was treated with MINOCIN (100 Mg; Qd; Oral) (View Minocin Review and Minocin Label ), SYMBICORT (View Symbicort Review and Symbicort Label ).

6836661-7 | Arthralgia, Dyspepsia, Hepatic Enzyme Increased, Meningitis Viral, Rash Pustular, Serum Sickness, Vomiting, White Blood Cell Count Decreased
Adverse event was reported on Jun 25, 2010 by a Female patient taking Omnaris (View Usage) (Dosage: Nasal) was diagnosed with dermatitis, lichen planus and. Location: UNITED STATES , 40 years of age, weighting 140.0 lb, Patient experienced the following unwanted or unexpected effects: arthralgia, dyspepsia, hepatic enzyme increased, meningitis viral, rash pustular, serum sickness, vomiting, white blood cell count decreased. During the same period patient was treated with MINOCIN (100 Mg;qd;oral; 200 Mg;qd;oral) (View Minocin Review and Minocin Label ).

6765901-8 | Activated Partial Thromboplastin Time Prolonged, Arrhythmia, Cardiomegaly, Deep Vein Thrombosis, Epistaxis, Fall, Fluid Retention, Hyponatraemia
on May 26, 2010 Male patient from , 81 years of age, weighting 162.9 lb, was diagnosed with rhinorrhoea and was treated with Omnaris (View Usage). Patient had the following side effects: activated partial thromboplastin time prolonged, arrhythmia (What is arrhythmia?), cardiomegaly, deep vein thrombosis (What is deep vein thrombosis?), epistaxis, fall (What is fall?), fluid retention, hyponatraemia. Omnaris dosage: Nasal, 200 Ug;bid;nasal, 1x; Nasal. During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), SINGULAIR (View Singulair Review and Singulair Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), DIURETICS (View Diuretics Review and Diuretics Label ), VITAMIN K /00854101/ (View Vitamin K /00854101/ Review and Vitamin K /00854101/ Label ). Patient was hospitalized.

6763848-4 | Dysgeusia, Dyspnoea, Panic Attack, Unevaluable Event
on May 27, 2010 Female patient from UNITED STATES , 29 years of age, was diagnosed with multiple allergies and was treated with Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: dysgeusia, dyspnoea, panic attack, unevaluable event. Omnaris dosage: 100 Mg 1x Nasal.

6761121-1 | Arrhythmia, Fall, Fluid Retention, Infection, Injury, Lethargy, Malaise, Rhinorrhoea
Patient was taking Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: arrhythmia (What is arrhythmia?), fall (What is fall?), fluid retention, infection (What is infection?), injury, lethargy, malaise, rhinorrhoea on May 21, 2010 from UNITED STATES Additional patient health information: Male patient , 81 years of age, weighting 162.9 lb, was diagnosed with rhinorrhoea and. Omnaris dosage: Nasal; 200 Ug;bid; Nasal. During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), SINGULAIR /01362601/ (View Singulair /01362601/ Review and Singulair /01362601/ Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), DIURETICS (View Diuretics Review and Diuretics Label ). Patient was hospitalized.

6731358-6 | Acne, Fungal Infection, Weight Increased
Adverse event was reported on May 17, 2010 by a Female patient taking Omnaris (View Usage) (Dosage: 2 Sprays Per Nostril Once A Day Nasal) was diagnosed with multiple allergies, sinusitis (What is sinusitis?) and. Location: UNITED STATES , 22 years of age, weighting 139.0 lb, Patient had the following side effects: acne (What is acne?), fungal infection (What is fungal infection?), weight increased.

6682816-4 | Nasal Congestion, Nasal Oedema, Status Asthmaticus
on Mar 30, 2010 Female patient from UNITED STATES , 43 years of age, was diagnosed with rhinitis allergic and was treated with Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: nasal congestion, nasal oedema, status asthmaticus. Omnaris dosage: 200 Ug; Qd; Nasal. During the same period patient was treated with NASACORT (View Nasacort Review and Nasacort Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label ). Patient was hospitalized.

6638667-X | Burning Sensation Mucosal, Headache, Sinus Congestion
on Mar 16, 2010 Female patient from UNITED STATES , weighting 200.0 lb, was diagnosed with nasal congestion and was treated with Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: burning sensation mucosal, headache (What is headache?), sinus congestion. Omnaris dosage: 2 Metered Sprays Once A Day Nasal. During the same period patient was treated with BENEDRIL (View Benedril Review and Benedril Label ).

6632630-0 | Dizziness, Face Injury, Fall, Impaired Work Ability, Loss Of Consciousness
Patient was taking Omnaris (View Usage). Patient had the following side effects: dizziness (What is dizziness?), face injury, fall (What is fall?), impaired work ability, loss of consciousness on Feb 24, 2010 from UNITED STATES Additional patient health information: Female patient , 69 years of age, was diagnosed with multiple allergies and. Omnaris dosage: 200 Ug; Qd; Nasal 200 Ug; 1x; Nasal. During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), VITAMINS (View Vitamins Review and Vitamins Label ), VITAMIN A (View Vitamin A Review and Vitamin A Label ), LOVAZA (View Lovaza Review and Lovaza Label ). Patient was hospitalized.

6619499-5 | Allergy To Plants, Asthma, Chronic Obstructive Pulmonary Disease, Condition Aggravated, Pneumonia, Product Measured Potency Issue
Adverse event was reported on Feb 19, 2010 by a Female patient taking Omnaris (View Usage) (Dosage: 100 Ug;prn; Nasal) was diagnosed with multiple allergies and. Location: UNITED STATES , 61 years of age, After Omnaris was administered, patient had the following side effects: allergy to plants, asthma (What is asthma?), chronic obstructive pulmonary disease, condition aggravated, pneumonia (What is pneumonia?), product measured potency issue. During the same period patient was treated with ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ). Patient was hospitalized.

6608580-2 | Face Injury, Presyncope
on Feb 26, 2010 Female patient from UNITED STATES , 69 years of age, weighting 123.0 lb, was diagnosed with seasonal allergy and was treated with Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: face injury, presyncope. Omnaris dosage: 2 Sprayseach Nostril 1x Per Day, Bedtim Nasal. Patient was hospitalized.

6558614-9 | Feeling Abnormal, Headache, Insomnia
on Jan 28, 2010 Female patient from UNITED STATES , 56 years of age, weighting 180.0 lb, was diagnosed with sinusitis (What is sinusitis?) and was treated with Omnaris (View Usage). Patient had the following side effects: feeling abnormal, headache (What is headache?), insomnia. Omnaris dosage: One Spray In Each Nostril Twice Daily Other.

6545517-9 | Supraventricular Tachycardia
Patient was taking Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: supraventricular tachycardia on Jan 04, 2010 from UNITED STATES Additional patient health information: Male patient , 67 years of age, weighting 167.1 lb, was diagnosed with rhinitis and. Omnaris dosage: 200 Ug;qd; Nasal. During the same period patient was treated with VERAPAMIL (CON.) (View Verapamil (con.) Review and Verapamil (con.) Label ), HYDROCHLOROTHIAZIDE (CON.) (View Hydrochlorothiazide (con.) Review and Hydrochlorothiazide (con.) Label ).

6530052-4 | Anosmia, Multiple Myeloma
Adverse event was reported on Nov 21, 2009 by a Male patient taking Omnaris (View Usage) (Dosage: 200 Ug; Nasal) was diagnosed with sinus disorder and. Location: UNITED STATES , 77 years of age, weighting 224.0 lb, Patient experienced the following unwanted or unexpected effects: anosmia, multiple myeloma (What is multiple myeloma?). During the same period patient was treated with GLYBURIDE (CON.) (View Glyburide (con.) Review and Glyburide (con.) Label ), METFORMIN (CON.) (View Metformin (con.) Review and Metformin (con.) Label ), FINASTERIDE (CON.) (View Finasteride (con.) Review and Finasteride (con.) Label ), ALLOPURINOL (CON.) (View Allopurinol (con.) Review and Allopurinol (con.) Label ), CENTRUM SILVER /01292501/ (CON.) (View Centrum Silver /01292501/ (con.) Review and Centrum Silver /01292501/ (con.) Label ), TYLENOL /00020001/ (CON.) (View Tylenol /00020001/ (con.) Review and Tylenol /00020001/ (con.) Label ), PREV MEDS (View Prev Meds Review and Prev Meds Label ).

6525914-8 | Chorioretinopathy, Stress
on Dec 08, 2009 Male patient from GERMANY , 46 years of age, was diagnosed with rhinitis and was treated with Omnaris (View Usage). Patient had the following side effects: chorioretinopathy, stress (What is stress?). Omnaris dosage: 200 Ug; Qd; Nasal. During the same period patient was treated with MICARDIS (View Micardis Review and Micardis Label ), CRESTOR /01588602/ (View Crestor /01588602/ Review and Crestor /01588602/ Label ).

6480269-2 | Cardiac Murmur
on Nov 20, 2009 Male patient from UNITED STATES , weighting 7.58 lb, was treated with Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: cardiac murmur. Omnaris dosage: . During the same period patient was treated with CON MEDS (View Con Meds Review and Con Meds Label ), PREV MEDS (View Prev Meds Review and Prev Meds Label ).

6456844-8 | Retinopathy
Patient was taking Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: retinopathy on Nov 04, 2009 from BRAZIL Additional patient health information: Male patient , 46 years of age, was diagnosed with rhinitis and. Omnaris dosage: 200 Ug; Qd; Nasal. During the same period patient was treated with MICARDIS (CON.) (View Micardis (con.) Review and Micardis (con.) Label ), CRESTOR /01588602/ (CON.) (View Crestor /01588602/ (con.) Review and Crestor /01588602/ (con.) Label ), PREV MEDS (View Prev Meds Review and Prev Meds Label ).

6409226-9 | Fatigue, Feeling Abnormal, Headache
Adverse event was reported on Oct 19, 2009 by a Female patient taking Omnaris (View Usage) (Dosage: Daily Nasal) was diagnosed with multiple allergies and. Location: UNITED STATES , 85 years of age, weighting 150.0 lb, Patient had the following side effects: fatigue, feeling abnormal, headache (What is headache?).

6397594-6 | Abdominal Discomfort, Angioedema, Bronchospasm, Chest Pain, Choking Sensation, Condition Aggravated, Cough, Decreased Appetite
on Sep 22, 2009 Female patient from UNITED STATES , 66 years of age, weighting 151.9 lb, was diagnosed with cough and was treated with Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: abdominal discomfort, angioedema, bronchospasm, chest pain (What is chest pain?), choking sensation, condition aggravated, cough, decreased appetite. Omnaris dosage: 200 Ug; 1x; Nasal. During the same period patient was treated with ZETIA (View Zetia Review and Zetia Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), SINGULAIR (View Singulair Review and Singulair Label ), OS CAL + D (View Os-cal + D Review and Os-cal + D Label ), AMBIEN (View Ambien Review and Ambien Label ). Patient was hospitalized.

6368625-4 | Acute Sinusitis, Bronchial Hyperreactivity, Dehydration, Dysphonia, Escherichia Urinary Tract Infection, Hyponatraemia
on Sep 02, 2009 Female patient from UNITED STATES , 58 years of age, was diagnosed with multiple allergies, nasal congestion and was treated with Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: acute sinusitis, bronchial hyperreactivity, dehydration, dysphonia, escherichia urinary tract infection, hyponatraemia. Omnaris dosage: 200 Ug; Qd; Nasal, 100 Ug; Qd; Nasal. During the same period patient was treated with ASTELIN (; Hs;) (View Astelin Review and Astelin Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), PROAIR HFA (View Proair Hfa Review and Proair Hfa Label ), TRAZODONE (View Trazodone Review and Trazodone Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ). Patient was hospitalized.

6357133-2 | Abdominal Discomfort, Angioedema, Asthma, Bronchospasm, Chest Pain, Choking Sensation, Cough, Decreased Appetite
Patient was taking Omnaris (View Usage). Patient had the following side effects: abdominal discomfort, angioedema, asthma (What is asthma?), bronchospasm, chest pain (What is chest pain?), choking sensation, cough, decreased appetite on May 28, 2009 from UNITED STATES Additional patient health information: Female patient , 66 years of age, weighting 151.9 lb, was diagnosed with cough and. Omnaris dosage: 200 Ug;1x;nasal. During the same period patient was treated with ZETIA (View Zetia Review and Zetia Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), SINGULAIR (View Singulair Review and Singulair Label ), OS CAL + D (View Os-cal + D Review and Os-cal + D Label ), AMBIEN (View Ambien Review and Ambien Label ). Patient was hospitalized.

6348638-9 | Dysphonia, Headache, Sinusitis, Urinary Tract Infection
Adverse event was reported on Aug 25, 2009 by a Female patient taking Omnaris (View Usage) (Dosage: 200 Ug; Qd; Nasal, 100 Ug; Qd; Nasal) was diagnosed with nasal congestion and. Location: UNITED STATES , 58 years of age, After Omnaris was administered, patient had the following side effects: dysphonia, headache (What is headache?), sinusitis (What is sinusitis?), urinary tract infection (What is urinary tract infection?). During the same period patient was treated with ASTELIN (; Hs;) (View Astelin Review and Astelin Label ), ADVAIR HFA (View Advair Hfa Review and Advair Hfa Label ), PROAIR HFA (View Proair Hfa Review and Proair Hfa Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ). Patient was hospitalized.

6317220-1 | Atrial Flutter
on Aug 06, 2009 Male patient from UNITED STATES , 51 years of age, weighting 185.0 lb, was diagnosed with nocturnal dyspnoea, seasonal allergy and was treated with Omnaris (View Usage). Patient experienced the following unwanted or unexpected effects: atrial flutter. Omnaris dosage: 200 Ug; Hs; Nasal. During the same period patient was treated with QUINAGLUTE (View Quinaglute Review and Quinaglute Label ), NEXIUM (View Nexium Review and Nexium Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), ZOCOR (View Zocor Review and Zocor Label ), WARFARIN (View Warfarin Review and Warfarin Label ).

6317219-5 | Asthma, Choking Sensation, Sinusitis
on May 28, 2009 Female patient from UNITED STATES , 66 years of age, weighting 151.9 lb, was diagnosed with cough and was treated with Omnaris (View Usage). Patient had the following side effects: asthma (What is asthma?), choking sensation, sinusitis (What is sinusitis?). Omnaris dosage: 200 Ug; 1x; Nasal. During the same period patient was treated with LEVOTHYROXINE (View Levothyroxine Review and Levothyroxine Label ), PROTONIX /01263201/ (View Protonix /01263201/ Review and Protonix /01263201/ Label ), ZETIA (View Zetia Review and Zetia Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ). Patient was hospitalized.

6230343-0 | Condition Aggravated, Cough, Sinusitis
Patient was taking Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: condition aggravated, cough, sinusitis (What is sinusitis?) on May 28, 2009 from UNITED STATES Additional patient health information: Female patient , 66 years of age, weighting 151.9 lb, was diagnosed with cough and. Omnaris dosage: 200 Ug; Ix; Nasal. During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), PROTONIX /01263201/ (View Protonix /01263201/ Review and Protonix /01263201/ Label ), ZETIA (View Zetia Review and Zetia Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ). Patient was hospitalized.

6087002-7 | Aphonia, Chest Pain, Dizziness, Dyspnoea, Hyperhidrosis, Muscle Fatigue, Nasal Congestion, Ocular Hyperaemia, Tremor
Adverse event was reported on Feb 11, 2009 by a Male patient taking Omnaris (View Usage) (Dosage: 100 Ug; Qd; Nasal) was diagnosed with sinusitis (What is sinusitis?) and. Location: UNITED STATES , 44 years of age, weighting 158.1 lb, Patient experienced the following unwanted or unexpected effects: aphonia, chest pain (What is chest pain?), dizziness (What is dizziness?), dyspnoea, hyperhidrosis, muscle fatigue, nasal congestion, ocular hyperaemia, tremor. During the same period patient was treated with XOPENEX (View Xopenex Review and Xopenex Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), PEPCID (View Pepcid Review and Pepcid Label ). Patient was hospitalized.

6063981-9 | Device Malfunction, Product Quality Issue
on Feb 03, 2009 Female patient from UNITED STATES , 55 years of age, was treated with Omnaris (View Usage). Patient had the following side effects: device malfunction, product quality issue. Omnaris dosage: 2 Sprays Per Nostril Daily..

5964718-1 | Tunnel Vision, Vision Blurred
on Nov 24, 2008 Male patient from UNITED STATES , 18 years of age, weighting 175.0 lb, was diagnosed with sinus disorder and was treated with Omnaris (View Usage). After Omnaris was administered, patient had the following side effects: tunnel vision, vision blurred. Omnaris dosage: 50mg 1 Daily Nasal.