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Betimol adverse events reported to FDA.

Have You Experienced unusual Betimol symptoms? PatientsVille.com collects and analyzes Betimol side effect and adverse reports submitted by Betimol users, such as .

Summary

FDA Adverse Reports: 6. View All

Betimol FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 2

Betimol Dosage, Warnings, Usage.

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

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6874716-1 | Pulmonary Embolism
on Jul 15, 2010 Female patient from UNITED STATES , 67 years of age, was diagnosed with open angle glaucoma, ocular hypertension and was treated with Betimol (View Usage). Patient experienced the following unwanted or unexpected effects: pulmonary embolism (What is pulmonary embolism?). Betimol dosage: , Bid, Ocular. During the same period patient was treated with STRENGTH: 0.25% OR 0.5%; MFR/LABELER: SANTEN OY (View Strength: 0.25% Or 0.5%; Mfr/labeler: Santen Oy Review and Strength: 0.25% Or 0.5%; Mfr/labeler: Santen Oy Label ), AMLODIPINE BESYLATE/BENAZEPRIL HYDRO (View Amlodipine Besylate/benazepril Hydro Review and Amlodipine Besylate/benazepril Hydro Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), INDAPAMIDE (View Indapamide Review and Indapamide Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

6868686-X | Application Site Pain, Lacrimation Increased, Nasal Congestion, Photophobia, Visual Acuity Reduced
Patient was taking Betimol (View Usage). Patient had the following side effects: application site pain, lacrimation increased, nasal congestion, photophobia, visual acuity reduced on Jul 21, 2010 from UNITED STATES Additional patient health information: Male patient , 56 years of age, weighting 120.0 lb, was diagnosed with glaucoma (What is glaucoma?) and. Betimol dosage: 1 Drop 2 Times A Day 5 Or 6 Month.

6286306-2 | Metastases To Bone, Renal Cancer Metastatic
Adverse event was reported on Jul 08, 2009 by a Male patient taking Betimol (View Usage) (Dosage: ) . Location: UNITED STATES , 80 years of age, After Betimol was administered, patient had the following side effects: metastases to bone, renal cancer metastatic.

6026677-5 |
on Dec 22, 2008 Female patient from UNITED STATES , 81 years of age, weighting 130.0 lb, was diagnosed with glaucoma (What is glaucoma?) and was treated with Betimol (View Usage). . Betimol dosage: One Drop; Both Eyes; Daily; Many Years.


5672438-6 | Urinary Tract Infection
on Mar 13, 2008 Female patient from UNITED STATES , weighting 197.0 lb, was diagnosed with glaucoma (What is glaucoma?) and was treated with Betimol (View Usage). Patient had the following side effects: urinary tract infection (What is urinary tract infection?). Betimol dosage: Bid; Each Eye Daily. During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), REMICADE (View Remicade Review and Remicade Label ). Patient was hospitalized.

4624227-9 | Heart Rate Increased
Patient was taking Betimol (View Usage). After Betimol was administered, patient had the following side effects: heart rate increased on Mar 30, 2005 from Additional patient health information: Female patient , weighting 100.0 lb, was diagnosed with glaucoma (What is glaucoma?) and. Betimol dosage: 1 Gtt Ou Bid (am + Pm) About 4 Weeks Ending On 3/9/05. During the same period patient was treated with NEXIUM (View Nexium Review and Nexium Label ), ACTONEL (View Actonel Review and Actonel Label ), M.V.I. (View M.v.i. Review and M.v.i. Label ), VITAMIN C (View Vitamin C Review and Vitamin C Label ), CALCIUM GLUCONATE (View Calcium Gluconate Review and Calcium Gluconate Label ), BETA CAROTENE (View Beta Carotene Review and Beta Carotene 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 Betimol 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 Betimol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Betimol 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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Betimol Reactions
Application Site Pain
Death
Heart Rate Increased
Lacrimation Increased
Metastases To Bone
Nasal Congestion
Photophobia
Pulmonary EmbolismWhat is Pulmonary embolism?
Renal Cancer Metastatic
Urinary Tract InfectionWhat is Urinary tract infection?
Visual Acuity Reduced
Betimol 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 Betimol 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!