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Weak Legs (2)
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Weak Legs And Imbalance (1)
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Common Acebutolol Side Effects

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Acebutolol adverse events reported to FDA.

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Summary

FDA Adverse Reports: 9. View All

Acebutolol FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 3

More About Acebutolol

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1Headache Sweating Frequent Urination
2Weak Legs
3Stomach Cramps. Vomiting
4Leg Ache
5Weak Legs And Imbalance
6Imbalance
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Often additional risks of using a medication, such as Acebutolol, 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 Acebutolol users, Learn more about unwanted side effects & find ways to reduce them. Browse Acebutolol Adverse Reports reported to FDA and participate in Acebutolol discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Acebutolol. 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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Acebutolol Adverse Effect Reports (FDA)

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6273014-7 | Blood Pressure Increased, Product Substitution Issue
on Jul 15, 2009 Male patient from UNITED STATES , weighting 218.0 lb, was diagnosed with hypertension and was treated with Acebutolol (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, product substitution issue. Acebutolol dosage: 1 Cap Qd Po.

6121301-5 | Arthralgia, Bone Pain, Inadequate Analgesia
Patient was taking Acebutolol (View Usage). Patient had the following side effects: arthralgia, bone pain, inadequate analgesia on Mar 12, 2009 from UNITED STATES Additional patient health information: Female patient , 67 years of age, weighting 165.0 lb, was diagnosed with supraventricular extrasystoles and. Acebutolol dosage: 200 Mg Twice Daily Po.

6100440-9 | Blood Pressure Inadequately Controlled, Product Quality Issue
Adverse event was reported on Feb 27, 2009 by a Female patient taking Acebutolol (View Usage) (Dosage: 200mg Twice Daily Other) was diagnosed with blood pressure (What is blood pressure?) and. Location: UNITED STATES , 34 years of age, After Acebutolol was administered, patient had the following side effects: blood pressure inadequately controlled, product quality issue.

5947849-1 | Cardio-respiratory Arrest, Completed Suicide
on Oct 23, 2008 Female patient from POLAND , 23 years of age, was treated with Acebutolol (View Usage). Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, completed suicide. Acebutolol dosage: ; Oral. During the same period patient was treated with NIFEDIPINE (; Oral) (View Nifedipine Review and Nifedipine Label ).


5947647-9 | Cardiac Disorder, Suicide Attempt, Therapeutic Agent Toxicity
on Oct 23, 2008 Female patient from POLAND , 19 years of age, was treated with Acebutolol (View Usage). Patient had the following side effects: cardiac disorder, suicide attempt, therapeutic agent toxicity. Acebutolol dosage: ; Oral. During the same period patient was treated with NIFEDIPINE (; Oral) (View Nifedipine Review and Nifedipine Label ).

5840293-7 | Blood Pressure Increased, Heart Rate Decreased, Heart Rate Irregular
Patient was taking Acebutolol (View Usage). After Acebutolol was administered, patient had the following side effects: blood pressure increased, heart rate decreased, heart rate irregular on Aug 08, 2008 from UNITED STATES Additional patient health information: Female patient , 67 years of age, weighting 142.0 lb, was diagnosed with extrasystoles, hypertension, anxiety (What is anxiety?) and. Acebutolol dosage: 200mg Once A Day Po. During the same period patient was treated with LORAZEPAM (1mg Three Times A Day Po, About 3 Years) (View Lorazepam Review and Lorazepam Label ).

5525396-9 | Chest Pain, Dyspnoea, Fatigue, Gait Disturbance, Headache, Hypertension, Hypotension, Impaired Work Ability, Insomnia
Adverse event was reported on Nov 05, 2007 by a Female patient taking Acebutolol (View Usage) (Dosage: 200 Mg; Daily; Oral) was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Location: UNITED STATES , 79 years of age, weighting 118.0 lb, Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), dyspnoea, fatigue, gait disturbance, headache (What is headache?), hypertension, hypotension, impaired work ability, insomnia. During the same period patient was treated with ACEBUTOLOL HCL (200 Mg; Daily; Oral) (View Acebutolol Hcl Review and Acebutolol Hcl Label ), MIRAPEX (View Mirapex Review and Mirapex Label ), COUMADIN (View Coumadin Review and Coumadin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PREMARIN (View Premarin Review and Premarin Label ), XANAX (View Xanax Review and Xanax Label ), ATACAND (View Atacand Review and Atacand Label ). Patient was hospitalized.

5273530-0 | Palpitations
on Mar 21, 2007 Female patient from UNITED STATES , 63 years of age, was treated with Acebutolol (View Usage). Patient had the following side effects: palpitations. Acebutolol dosage: .

5143865-0 | Pain In Extremity
on Nov 02, 2006 Female patient from UNITED STATES , weighting 141.0 lb, was diagnosed with hypertension and was treated with Acebutolol (View Usage). After Acebutolol was administered, patient had the following side effects: pain in extremity. Acebutolol dosage: 400 Mg 1 Q Day Oral.


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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 Acebutolol 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 Acebutolol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Acebutolol 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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Acebutolol Reactions
Arthralgia
Blood Pressure Inadequately Controlled
Blood Pressure Increased
Bone Pain
Cardiac Disorder
Cardio-respiratory Arrest
Chest PainWhat is Chest pain?
Completed Suicide
Dyspnoea
Fatigue
Gait Disturbance
HeadacheWhat is Headache?
Heart Rate Decreased
Heart Rate Irregular
Hypertension
Hypotension
Impaired Work Ability
Inadequate Analgesia
Insomnia
Pain In Extremity
Palpitations
Product Quality Issue
Product Substitution Issue
Suicide Attempt
Therapeutic Agent Toxicity
Acebutolol 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 Acebutolol 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!