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Flunisolide adverse events reported to FDA.

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Summary

FDA Adverse Reports: 23. View All

Flunisolide FDA safety alerts: No

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Flunisolide, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Flunisolide users, Learn more about unwanted side effects & find ways to reduce them. Browse Flunisolide Adverse Reports reported to FDA and participate in Flunisolide discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Flunisolide. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Flunisolide Adverse Effect Reports (FDA)

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6856344-7 | Eye Pain, Lacrimation Increased, Nasal Discomfort, Product Substitution Issue
on Jul 15, 2010 Female patient from UNITED STATES , 61 years of age, weighting 300.0 lb, was diagnosed with multiple allergies and was treated with Flunisolide (View Usage). Patient experienced the following unwanted or unexpected effects: eye pain, lacrimation increased, nasal discomfort, product substitution issue. Flunisolide dosage: 2 Sprays In Each Nostril 2 Times A Day Nasal.

6811496-X | Apathy, Back Pain, Cognitive Disorder, Condition Aggravated, Crying, Depression, Diabetes Mellitus, Disturbance In Attention, Fall
Patient was taking Flunisolide (View Usage). Patient had the following side effects: apathy, back pain (What is back pain?), cognitive disorder, condition aggravated, crying, depression (What is depression?), diabetes mellitus, disturbance in attention, fall (What is fall?) on Jun 12, 2010 from UNITED STATES Additional patient health information: Male patient , 87 years of age, was diagnosed with rhinitis allergic, depression (What is depression?) and. Flunisolide dosage: . During the same period patient was treated with CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ).

6656602-5 | Ageusia, Anosmia, Decreased Appetite, Dysgeusia, Tooth Deposit
Adverse event was reported on Feb 04, 2010 by a Male patient taking Flunisolide (View Usage) (Dosage: ) was diagnosed with sinus congestion, polyuria and. Location: UNITED STATES , 62 years of age, After Flunisolide was administered, patient had the following side effects: ageusia, anosmia, decreased appetite, dysgeusia, tooth deposit. During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), BUMEX (View Bumex Review and Bumex Label ).

6656601-3 | Epistaxis, Face Injury
on Oct 29, 2009 Female patient from UNITED STATES , 68 years of age, was diagnosed with seasonal allergy and was treated with Flunisolide (View Usage). Patient experienced the following unwanted or unexpected effects: epistaxis, face injury. Flunisolide dosage: . During the same period patient was treated with CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), VITAMIN K TAB (View Vitamin K Tab Review and Vitamin K Tab Label ), ZINC (View Zinc Review and Zinc Label ), POTASSIUM (View Potassium Review and Potassium Label ).


6656600-1 | Nasal Discomfort
on Sep 25, 2009 Male patient from UNITED STATES , 41 years of age, was diagnosed with hypersensitivity, hypertension and was treated with Flunisolide (View Usage). Patient had the following side effects: nasal discomfort. Flunisolide dosage: . During the same period patient was treated with ZYRTEC D 12 HOUR (View Zyrtec-d 12 Hour Review and Zyrtec-d 12 Hour Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ).

6581877-0 | Convulsion, Cough, Syncope, Wheezing
Patient was taking Flunisolide (View Usage). After Flunisolide was administered, patient had the following side effects: convulsion, cough, syncope, wheezing on Feb 12, 2010 from UNITED STATES Additional patient health information: Male patient , 64 years of age, weighting 209.2 lb, was diagnosed with chronic obstructive pulmonary disease and. Flunisolide dosage: .

6436549-X | Asthenia, Dizziness, Paraesthesia
Adverse event was reported on Nov 10, 2009 by a Male patient taking Flunisolide (View Usage) (Dosage: 2 Puff(s) Bid Nasal) was diagnosed with nasal congestion and. Location: UNITED STATES , 64 years of age, weighting 229.0 lb, Patient experienced the following unwanted or unexpected effects: asthenia, dizziness (What is dizziness?), paraesthesia.

6431129-4 | Candidiasis
on Nov 05, 2009 Male patient from UNITED STATES , 80 years of age, weighting 127.9 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with Flunisolide (View Usage). Patient had the following side effects: candidiasis. Flunisolide dosage: . During the same period patient was treated with MOMETASONE FUROATE (View Mometasone Furoate Review and Mometasone Furoate Label ).

6231072-X | Epistaxis
on Jun 12, 2009 Male patient from UNITED STATES , 59 years of age, weighting 241.0 lb, was diagnosed with rhinitis allergic and was treated with Flunisolide (View Usage). After Flunisolide was administered, patient had the following side effects: epistaxis. Flunisolide dosage: 2 Puff(s) Every Day Nasal.

6219197-6 | Condition Aggravated, Postnasal Drip, Product Substitution Issue
Patient was taking Flunisolide (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, postnasal drip, product substitution issue on Jun 05, 2009 from UNITED STATES Additional patient health information: Male patient , 62 years of age, weighting 155.0 lb, was diagnosed with rhinitis allergic and. Flunisolide dosage: 2 Sprays Bid Nasal.

5775432-X | Acute Myocardial Infarction, Anorexia, Dehydration, Impaired Gastric Emptying, Nausea, Oral Intake Reduced
Adverse event was reported on Jun 02, 2008 by a Male patient taking Flunisolide (View Usage) (Dosage: ) was diagnosed with fatigue and. Location: UNITED STATES , 86 years of age, Patient had the following side effects: acute myocardial infarction, anorexia, dehydration, impaired gastric emptying, nausea (What is nausea?), oral intake reduced. During the same period patient was treated with SALBUTAMOL (ALBUTEROL) (View Salbutamol (albuterol) Review and Salbutamol (albuterol) Label ), IPRATROPIUM BROMIDE (View Ipratropium Bromide Review and Ipratropium Bromide Label ), MOMETASONE (MOMETASONE) (View Mometasone (mometasone) Review and Mometasone (mometasone) Label ), DENEZEPIL (10 Mg) (View Denezepil Review and Denezepil Label ), CYPROHEPTADINE HCL (4 Mg Qd) (View Cyproheptadine Hcl Review and Cyproheptadine Hcl Label ), FAMOTIDINE (40 Mg Qd) (View Famotidine Review and Famotidine Label ), FUROSEMIDE (20 Mg Tiw) (View Furosemide Review and Furosemide Label ), ISOSORBIDE MONONITRATE (15 Mg Qd) (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ). Patient was hospitalized.

5639063-4 | Eye Pruritus, Eyelid Oedema, Nasal Congestion, Nasal Discomfort
on Feb 16, 2007 Male patient from UNITED STATES , 44 years of age, was diagnosed with nasal polyps, headache (What is headache?), arthritis (What is arthritis?) and was treated with Flunisolide (View Usage). After Flunisolide was administered, patient had the following side effects: eye pruritus, eyelid oedema, nasal congestion, nasal discomfort. Flunisolide dosage: .

5512620-1 | Mucosal Dryness
on Nov 08, 2007 Male patient from UNITED STATES , 40 years of age, weighting 202.6 lb, was treated with Flunisolide (View Usage). Patient experienced the following unwanted or unexpected effects: mucosal dryness. Flunisolide dosage: .

5507725-5 | Liver Disorder, Malaise
Patient was taking Flunisolide (View Usage). Patient had the following side effects: liver disorder, malaise on Nov 05, 2007 from UNITED STATES Additional patient health information: Male patient , 54 years of age, weighting 159.0 lb, was diagnosed with mycotic allergy and. Flunisolide dosage: 2 Spays Each Nostril Twice A Day Nasal.

5465421-7 | Epistaxis, Nasal Discomfort
Adverse event was reported on Sep 20, 2007 by a Male patient taking Flunisolide (View Usage) (Dosage: 50mcg Bid Nasal) . Location: UNITED STATES , 72 years of age, After Flunisolide was administered, patient had the following side effects: epistaxis, nasal discomfort.

5463083-6 | Palpitations
on Sep 18, 2007 Male patient from UNITED STATES , 29 years of age, was diagnosed with rhinitis allergic and was treated with Flunisolide (View Usage). Patient experienced the following unwanted or unexpected effects: palpitations. Flunisolide dosage: .

5463082-4 | Nasal Discomfort
on Sep 18, 2007 Male patient from UNITED STATES , 71 years of age, was diagnosed with rhinitis allergic and was treated with Flunisolide (View Usage). Patient had the following side effects: nasal discomfort. Flunisolide dosage: 2puff(2) Bid Nasal.

5374649-6 | Nasal Congestion, Nasal Discomfort, Snoring
Patient was taking Flunisolide (View Usage). After Flunisolide was administered, patient had the following side effects: nasal congestion, nasal discomfort, snoring (What is snoring?) on Jun 27, 2007 from UNITED STATES Additional patient health information: Male patient , 61 years of age, was diagnosed with rhinitis allergic and. Flunisolide dosage: 1puff(s) Bid Nasal.

5291957-8 | Nasal Discomfort, Nasal Dryness, Nasal Mucosal Disorder
Adverse event was reported on Apr 06, 2007 by a Female patient taking Flunisolide (View Usage) (Dosage: ) . Location: UNITED STATES , 76 years of age, weighting 227.1 lb, Patient experienced the following unwanted or unexpected effects: nasal discomfort, nasal dryness, nasal mucosal disorder.

5235187-4 | Epistaxis, Nasal Discomfort
on Feb 08, 2007 Male patient from UNITED STATES , 42 years of age, was diagnosed with postnasal drip, rhinorrhoea and was treated with Flunisolide (View Usage). Patient had the following side effects: epistaxis, nasal discomfort. Flunisolide dosage: 2 Puffs Qd.

4778171-7 | Headache
on Sep 23, 2005 Male patient from UNITED STATES , 67 years of age, weighting 199.1 lb, was treated with Flunisolide (View Usage). After Flunisolide was administered, patient had the following side effects: headache (What is headache?). Flunisolide dosage: . During the same period patient was treated with FOSINOPRIL (View Fosinopril Review and Fosinopril Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), GLYBURIDE (View Glyburide Review and Glyburide Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ROSIGLITAZONE MALEATE (View Rosiglitazone Maleate Review and Rosiglitazone Maleate Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

4682188-0 | Epistaxis
Patient was taking Flunisolide (View Usage). Patient experienced the following unwanted or unexpected effects: epistaxis on Jun 03, 2005 from Additional patient health information: Male patient , 71 years of age, weighting 171.3 lb, was diagnosed with rhinitis allergic and. Flunisolide dosage: 2 Sprays Each Nostril Bid. During the same period patient was treated with BRIMONIDE TARTRATE (View Brimonide Tartrate Review and Brimonide Tartrate Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), TRAVOPROST (View Travoprost Review and Travoprost Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ). Patient was hospitalized.

4682188-0 | Epistaxis
Adverse event was reported on Jun 03, 2005 by a Male patient taking Flunisolide (View Usage) (Dosage: 2 Sprays Each Nostril Bid) was diagnosed with rhinitis allergic and. Location: UNITED STATES , 71 years of age, weighting 171.3 lb, Patient had the following side effects: epistaxis. During the same period patient was treated with BRIMONIDE TARTRATE (View Brimonide Tartrate Review and Brimonide Tartrate Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), TRAVOPROST (View Travoprost Review and Travoprost Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ). Patient was hospitalized.


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Flunisolide Questions, Answers, Feedback and Comments

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Flunisolide risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Flunisolide quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Flunisolide use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Flunisolide Reactions
Acute Myocardial Infarction
Ageusia
Anorexia
Anosmia
Apathy
Asthenia
Back PainWhat is Back pain?
Candidiasis
Cognitive Disorder
Condition Aggravated
Convulsion
Cough
Crying
Decreased Appetite
Dehydration
DepressionWhat is Depression?
Diabetes Mellitus
Disturbance In Attention
DizzinessWhat is Dizziness?
Dysgeusia
Epistaxis
Eye Pain
Eye Pruritus
Eyelid Oedema
Face Injury
FallWhat is Fall?
HeadacheWhat is Headache?
Nasal Congestion
Nasal Discomfort
Product Substitution Issue
Flunisolide Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Flunisolide adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!