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Beloc adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Beloc FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 32

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

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5278267-X | Bradyarrhythmia
on Mar 16, 2007 Male patient from GERMANY , 64 years of age, was diagnosed with hypertension and was treated with Beloc (View Usage). Patient experienced the following unwanted or unexpected effects: bradyarrhythmia. Beloc dosage: . During the same period patient was treated with VALSARTAN AND HYDROCHLOROTHIAZIDE (1 Df, Qd) (View Valsartan And Hydrochlorothiazide Review and Valsartan And Hydrochlorothiazide Label ).

5158431-0 | Blood Creatinine Increased, Body Temperature Increased, Bradyphrenia, C-reactive Protein Increased, Convulsion, Incontinence, Loss Of Consciousness, Muscle Twitching
Patient was taking Beloc (View Usage). Patient had the following side effects: blood creatinine increased, body temperature increased, bradyphrenia, c-reactive protein increased, convulsion, incontinence, loss of consciousness, muscle twitching on Nov 17, 2006 from SWEDEN Additional patient health information: Female patient , 45 years of age, . Beloc dosage: 95 Mg/day. During the same period patient was treated with LOCOL (40 Mg/day) (View Locol Review and Locol Label ), CITALOPRAM HYDROBROMIDE (40 Mg/day) (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), NEUROCIL (200 Mg/day) (View Neurocil Review and Neurocil Label ), TRIMIPRAMINE MALEATE (150 Mg/day) (View Trimipramine Maleate Review and Trimipramine Maleate Label ), TAXILAN (500 Mg/day) (View Taxilan Review and Taxilan Label ). Patient was hospitalized.


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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 Beloc 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 Beloc quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Beloc 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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How Did You Deal with Side Effects?

Beloc-zok Side Effects - Complete Patient's Guide | User Reviews: Female patient, 45 years of age, weighting 132.3

... Insulin Review and Insulin Label ), DELIX (2.5 Mg, Qd) (View Delix Review and Delix Label ), BELOC ZOK (50 Mg, Qd) (View Beloc Zok Review and Beloc Zok Label ), PRAVACHOL (10 ...

During the same period patient was treated with BELOC ZOK (View Beloc-zok Review and Beloc-zok Label ), BELOC ZOK (View Beloc-zok Review and Beloc-zok Label ), PANTOZOL (View ...

)During the same period patient was treated with BELOC (View Beloc Review and Beloc Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), PREDNISONE TAB (View ...

During the same period patient was treated with AMPICILLIN AND SULBACTAM (3g Per Day) (View Ampicillin And Sulbactam Review and Ampicillin And Sulbactam Label ), BELOC ZOK ...

beloc Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: coversum Episodes: 1: Diagnosed with major depression.Side ...

... D),oral) (View Gabapentin Review and Gabapentin Label ), BENZBROMARONE AL (100 Mg (100 Mg,1 In 1 D),oral) (View Benzbromarone Al Review and Benzbromarone Al Label ), BELOC ...

During the same period patient was treated with FLOXACILLIN, ASPIRIN CARDIO, CLEXANE, SIMVASTATIN, NEXIUM, LANTUS, BELOC, DAFALGAN. Patient was hospitalized.

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Beloc Reactions
Blood Creatinine Increased
Body Temperature Increased
Bradyarrhythmia
Bradyphrenia
C-reactive Protein Increased
Convulsion
Incontinence
Loss Of Consciousness
Muscle Twitching
Beloc 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 Beloc 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!