Bonalon Side Effects

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Bonalon adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 4. View All

Bonalon FDA safety alerts: No

Reported hospitalizations: 1

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

5492279-2 | Liver Disorder
on Oct 12, 2007 Female patient from JAPAN , weighting 88.18 lb, was diagnosed with osteoporosis (What is osteoporosis?), peripheral circulatory failure, hypertension, cerebral infarction and was treated with Bonalon (View Usage). Patient experienced the following unwanted or unexpected effects: liver disorder. Bonalon dosage: Unk. During the same period patient was treated with JUVELA N (Unk) (View Juvela N Review and Juvela N Label ), DIOVAN (View Diovan Review and Diovan Label ), PLAVIX (View Plavix Review and Plavix Label ), D ALFA (View D-alfa Review and D-alfa Label ).

5453905-7 | Liver Disorder
Patient was taking Bonalon (View Usage). Patient had the following side effects: liver disorder on Sep 11, 2007 from JAPAN Additional patient health information: Female patient , weighting 88.18 lb, was diagnosed with osteoporosis (What is osteoporosis?), peripheral circulatory failure, hypertension, cerebral infarction and. Bonalon dosage: Unk. During the same period patient was treated with JUVELA N (Unk) (View Juvela N Review and Juvela N Label ), DIOVAN (View Diovan Review and Diovan Label ), PLAVIX (View Plavix Review and Plavix Label ), D ALFA (View D-alfa Review and D-alfa Label ).

5299492-8 | Hypothermia, Loss Of Consciousness
Adverse event was reported on Apr 05, 2007 by a Female patient taking Bonalon (View Usage) (Dosage: Unk) was diagnosed with circadian rhythm sleep disorder and. Location: JAPAN , 73 years of age, After Bonalon was administered, patient had the following side effects: hypothermia (What is hypothermia?), loss of consciousness. During the same period patient was treated with MYSLEE (5 Mg) (View Myslee Review and Myslee Label ).

4785206-4 | Mucosal Erosion, Rash
on Sep 14, 2005 Female patient from JAPAN , 72 years of age, was diagnosed with osteoporosis (What is osteoporosis?), hallucination, parkinson's disease (What is parkinson's disease?), constipation (What is constipation?), hypoaesthesia and was treated with Bonalon (View Usage). Patient experienced the following unwanted or unexpected effects: mucosal erosion, rash (What is rash?). Bonalon dosage: . During the same period patient was treated with GRAMALIL (View Gramalil Review and Gramalil Label ), CLINORIL (View Clinoril Review and Clinoril Label ), MADOPAR (View Madopar Review and Madopar Label ), ALFAROL (View Alfarol Review and Alfarol Label ), CALCIUM ASPARTATE (View Calcium Aspartate Review and Calcium Aspartate Label ), GLAKAY (View Glakay Review and Glakay Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), CYANOCOBALAMIN (View Cyanocobalamin Review and Cyanocobalamin 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 Bonalon 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 Bonalon quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Bonalon 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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BONALON Side Effects

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Bonalon Reactions

Hypothermia	What is Hypothermia?
Liver Disorder
Loss Of Consciousness
Mucosal Erosion
Rash	What is Rash?

BONALON Side Effects

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Bonalon adverse events reported to FDA.

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Bonalon Adverse Effect Reports (FDA)

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Bonalon Reactions