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Benet adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Benet FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 4

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

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5120494-6 | Fall, Loss Of Consciousness
on Aug 08, 2006 Female patient from JAPAN , 82 years of age, was diagnosed with osteoporosis (What is osteoporosis?), insomnia and was treated with Benet (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), loss of consciousness. Benet dosage: 2.5 Mg. During the same period patient was treated with ZOLPIDEM TARTRATE (5 Mg) (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ). Patient was hospitalized.

5102846-3 | Fall, Loss Of Consciousness
Patient was taking Benet (View Usage). Patient had the following side effects: fall (What is fall?), loss of consciousness on Aug 08, 2006 from JAPAN Additional patient health information: Female patient , 82 years of age, . Benet dosage: 2.5 Mg. During the same period patient was treated with MYSLEE (5 Mg) (View Myslee Review and Myslee 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 Benet 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 Benet quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Benet 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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Natrilix Side Effects - Complete Patient's Guide | User Reviews: Female patient, 65 years of age, was diagnosed |Side Effect|Coughing|Gout|Swollen Ankels Can This Be ...

During the same period patient was treated with ONEALFA (Unk) (View Onealfa Review and Onealfa Label ), BENET (Unk) (View Benet Review and Benet Label ), TALION (Unk) (View ...

... 15 Df, Unk) (View Predonine Review and Predonine Label ), BAKTAR (4 Df, Unk) (View Baktar Review and Baktar Label ), BENET (17.5 Df, Unk) (View Benet Review and Benet Label ...

During the same period patient was treated with BENET. Fosamax Side Effects Report: 6228070-9,Abdominal Pain, Anxiety, Asthenia, Blood Cholesterol Increased, Breast Mass ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

... 5mg Per Day) (View Norvasc Review and Norvasc Label ), CETAPRIL (50mg Per Day) (View Cetapril Review and Cetapril Label ), BENET (2.5mg Per Day) (View Benet Review and Benet ...

... Dose Reported As 200mg/m^2) (View Paclitaxel Review and Paclitaxel Label ), ALIMTA (View Alimta Review and Alimta Label ), BENET (View Benet Review and Benet Label

During the same period patient was treated with RHEUMATREX (View Rheumatrex Review and Rheumatrex Label ), FOLIAMIN (View Foliamin Review and Foliamin Label ), BENET (View ...

... Norvasc Label ), BLOPRESS (Unk) (View Blopress Review and Blopress Label ), MYSLEE (View Myslee Review and Myslee Label ), BENET (Unk) (View Benet Review and Benet Label ), ...

... Loxonin Review and Loxonin Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), OMEPRAL (View Omepral Review and Omepral Label ), BENET (View Benet Review and Benet Label ).

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Benet 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 Benet 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!