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Summary

FDA Adverse Reports: 7. View All

Brimonidine FDA safety alerts: No

Reported hospitalizations: 6

Brimonidine Dosage, Warnings, Usage.

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Often additional risks of using a medication, such as Brimonidine, 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 Brimonidine users, Learn more about unwanted side effects & find ways to reduce them. Browse Brimonidine Adverse Reports reported to FDA and participate in Brimonidine discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Brimonidine. 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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Brimonidine Adverse Effect Reports (FDA)

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6977431-9 | Conjunctivitis, Uveitis
on Aug 29, 2010 Male patient from UNITED STATES , 83 years of age, was diagnosed with open angle glaucoma and was treated with Brimonidine (View Usage). Patient experienced the following unwanted or unexpected effects: conjunctivitis, uveitis. Brimonidine dosage: .

6736532-0 | Nephropathy Toxic, Renal Impairment
Patient was taking Brimonidine (View Usage). Patient had the following side effects: nephropathy toxic, renal impairment on May 10, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 88 years of age, weighting 143.3 lb, was diagnosed with glaucoma (What is glaucoma?), atrial fibrillation (What is atrial fibrillation?), anaemia, constipation (What is constipation?) and. Brimonidine dosage: . During the same period patient was treated with DORZOLAMIDE (View Dorzolamide Review and Dorzolamide Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), BIMATOPROST AND TIMOLOL MALEATE (View Bimatoprost And Timolol Maleate Review and Bimatoprost And Timolol Maleate Label ), NULYTELY (View Nulytely Review and Nulytely Label ).

6722061-7 | Nephropathy Toxic, Renal Impairment
Adverse event was reported on May 05, 2010 by a Male patient taking Brimonidine (View Usage) (Dosage: ) was diagnosed with glaucoma (What is glaucoma?), atrial fibrillation (What is atrial fibrillation?), anaemia, constipation (What is constipation?) and. Location: UNITED KINGDOM , 88 years of age, weighting 143.3 lb, After Brimonidine was administered, patient had the following side effects: nephropathy toxic, renal impairment. During the same period patient was treated with DORZOLAMIDE (View Dorzolamide Review and Dorzolamide Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), GANFORT (BIMATOPROST, TIMOLOL) (View Ganfort (bimatoprost, Timolol) Review and Ganfort (bimatoprost, Timolol) Label ), NULYTELY (View Nulytely Review and Nulytely Label ).

6714305-2 | Nephropathy Toxic
on Apr 22, 2010 Male patient from UNITED KINGDOM , 88 years of age, weighting 143.3 lb, was diagnosed with glaucoma (What is glaucoma?), atrial fibrillation (What is atrial fibrillation?), anaemia, constipation (What is constipation?) and was treated with Brimonidine (View Usage). Patient experienced the following unwanted or unexpected effects: nephropathy toxic. Brimonidine dosage: . During the same period patient was treated with DORZOLAMIDE (View Dorzolamide Review and Dorzolamide Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), BIMATOPROST AND TIMOLOL MALEATE (View Bimatoprost And Timolol Maleate Review and Bimatoprost And Timolol Maleate Label ), MOVICOL (View Movicol Review and Movicol Label ).


6699221-7 | Nephropathy Toxic
on Apr 16, 2010 Male patient from UNITED KINGDOM , 88 years of age, weighting 143.3 lb, was diagnosed with glaucoma (What is glaucoma?), atrial fibrillation (What is atrial fibrillation?), anaemia, constipation (What is constipation?) and was treated with Brimonidine (View Usage). Patient had the following side effects: nephropathy toxic. Brimonidine dosage: . During the same period patient was treated with DORZOLAMIDE (View Dorzolamide Review and Dorzolamide Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), GANFORT (BIMATOPROST, TIMOLOL) (View Ganfort (bimatoprost, Timolol) Review and Ganfort (bimatoprost, Timolol) Label ), MOVICOL (View Movicol Review and Movicol Label ).

6296408-2 | Asthma, Hypersensitivity
Patient was taking Brimonidine (View Usage). After Brimonidine was administered, patient had the following side effects: asthma (What is asthma?), hypersensitivity on Jul 23, 2009 from UNITED KINGDOM Additional patient health information: Male patient , 56 years of age, was diagnosed with eye operation, eye inflammation and. Brimonidine dosage: . During the same period patient was treated with DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), PREDNISOLONE SODIUM PHOSPHATE (View Prednisolone Sodium Phosphate Review and Prednisolone Sodium Phosphate Label ), TOBRAMYCIN (View Tobramycin Review and Tobramycin Label ). Patient was hospitalized.

5983117-X | Iris Convex, Maculopathy, Retinal Detachment, Retinal Disorder, Retinal Pigment Epitheliopathy
Adverse event was reported on Nov 24, 2008 by a Male patient taking Brimonidine (View Usage) (Dosage: ) was diagnosed with ocular hypertension and. Location: UNITED STATES , 49 years of age, Patient experienced the following unwanted or unexpected effects: iris convex, maculopathy, retinal detachment, retinal disorder (What is retinal disorder?), retinal pigment epitheliopathy. During the same period patient was treated with TIMOLOL (View Timolol Review and Timolol Label ), DORZOLAMIDE W/TIMOLOL (View Dorzolamide W/timolol Review and Dorzolamide W/timolol Label ), APRACLONIDINE (View Apraclonidine Review and Apraclonidine Label ), TRAVOPROST (View Travoprost Review and Travoprost Label ).


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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 Brimonidine 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 Brimonidine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Brimonidine 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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Assessing the Efficacy and Tolerability of AZARGA® (Brinzolamide 1%/Timolol 0.5% Fixed Combination) as Replacement Therapy in Patients on COMBIGAN® (Brimonidine

Exelon Side Effects - Complete Patient's Guide | User Reviews: Female patient, weighting 88.18 lb, was diagnosed with |Doubled Up On Dose By Accident Will It Dpo Me ...

Assessing the Efficacy and Tolerability of AZARGA® (Brinzolamide 1%/Timolol 0.5% Fixed Combination) as Replacement Therapy in Patients on COMBIGAN® (Brimonidine

During the same period patient was treated with TIMOLOL (0.5 %, 2x/day) (View Timolol Review and Timolol Label ), BRIMONIDINE (0.2 %, 2x/day) (View Brimonidine Review and ...

Casodex Side Effects - Complete Patient's Guide | User Reviews: Male patient, 74 years of age, was diagnosed

During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), BRIMONIDINE TARTRATE (View Brimonidine Tartrate Review and Brimonidine ...

During the same period patient was treated with BRIMONIDINE 0.1% SOL W/ PURITE (View Brimonidine 0.1% Sol W/ Purite Review and Brimonidine 0.1% Sol W/ Purite Label ), ...

During the same period patient was treated with ATENOLOL, PERINDOPRIL ERBUMINE, METFORMIN, ATORVASTATIN CALCIUM, HYDROCORTISONE, BRIMONIDINE, BRIMONIDINE TARTRATE, ...

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Brimonidine Reactions
AsthmaWhat is Asthma?
Conjunctivitis
Hypersensitivity
Iris Convex
Maculopathy
Nephropathy Toxic
Renal Impairment
Retinal Detachment
Retinal DisorderWhat is Retinal disorder?
Retinal Pigment Epitheliopathy
Uveitis
Brimonidine 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 Brimonidine 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!