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Buflomedil adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Buflomedil FDA safety alerts: No

Reported hospitalizations: 4

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

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6857307-8 | Prothrombin Level Decreased, Thrombocytopenia
on Jul 05, 2010 Male patient from FRANCE , 81 years of age, was treated with Buflomedil (View Usage). Patient experienced the following unwanted or unexpected effects: prothrombin level decreased, thrombocytopenia. Buflomedil dosage: . During the same period patient was treated with PENTOXIFYLLINE (View Pentoxifylline Review and Pentoxifylline Label ), TAMSULOSIN HCL (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), RETIDIA (View Retidia Review and Retidia Label ). Patient was hospitalized.

6857305-4 | Haematoma, Hip Fracture, Prothrombin Level Decreased, Renal Failure Acute, Thrombocytopenia
Patient was taking Buflomedil (View Usage). Patient had the following side effects: haematoma, hip fracture, prothrombin level decreased, renal failure acute, thrombocytopenia on Jul 05, 2010 from FRANCE Additional patient health information: Male patient , 81 years of age, . Buflomedil dosage: . During the same period patient was treated with PENTOXIFYLLINE (View Pentoxifylline Review and Pentoxifylline Label ), TAMSULOSIN HCL (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), RETIDIA (View Retidia Review and Retidia Label ). Patient was hospitalized.

6649815-X | Clonus, Tremor
Adverse event was reported on Mar 10, 2010 by a Male patient taking Buflomedil (View Usage) (Dosage: ) was diagnosed with diabetes mellitus and. Location: FRANCE , 81 years of age, weighting 163.1 lb, After Buflomedil was administered, patient had the following side effects: clonus, tremor. During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), MONOTILDIEM /00489701/ (View Monotildiem /00489701/ Review and Monotildiem /00489701/ Label ), ATACAND (View Atacand Review and Atacand Label ), DAONIL (View Daonil Review and Daonil Label ), PLAVIX (View Plavix Review and Plavix Label ), BECOTIDE (View Becotide Review and Becotide Label ), BRONCHODUAL (View Bronchodual Review and Bronchodual Label ), SPIRIVA (View Spiriva Review and Spiriva Label ). Patient was hospitalized.

6544032-6 | Bradycardia, Hypotension
on Jan 06, 2010 Female patient from FRANCE , 86 years of age, was treated with Buflomedil (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, hypotension. Buflomedil dosage: . During the same period patient was treated with ZOLPIDEM (View Zolpidem Review and Zolpidem Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), ALDACTAZINE (View Aldactazine Review and Aldactazine Label ), ARICEPT (View Aricept Review and Aricept Label ), VITABACT (View Vitabact Review and Vitabact Label ). Patient was hospitalized.


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Buflomedil Questions, Answers, Feedback and Comments

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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 Buflomedil 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 Buflomedil quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Buflomedil 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?

During the same period patient was treated with ALTEIS (View Alteis Review and Alteis Label ), PARIET (View Pariet Review and Pariet Label ), BUFLOMEDIL (Unk) (View Buflomedil ...

... Piracetam Review and Piracetam Label ), CANDESARTAN (View Candesartan Review and Candesartan Label ), BUFLOMEDIL (View Buflomedil Review and Buflomedil Label ).

During the same period patient was treated with BUFLOMEDIL (TABLET) (BUFLOMEDIL) (Dosage Forms (1 Dosage Forms, 1 In 1 D), Oral/years) (View Buflomedil (tablet ...

... was treated with TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), BUFLOMEDIL (BUFLOMEDIL) (View Buflomedil ...

During the same period patient was treated with BUFLOMEDIL (3 Unk) (View Buflomedil Review and Buflomedil Label ), PLAVIX (View Plavix Review and Plavix Label ).

During the same period patient was treated with ALTEIS (View Alteis Review and Alteis Label ), PARIET (View Pariet Review and Pariet Label ), BUFLOMEDIL (Unk) (View ...

(View Buflomedil Review and Buflomedil Label ), SEROPRAM (View Seropram Review and Seropram Label ), PLAVIX ... Transipeg Side Effects Dafalgan Codeine Side Effects ...

... Being Less Than A Month.) (View Eupressyl Review and Eupressyl Label ), ATACAND (Reported As Being Less Than A Month.) (View Atacand Review and Atacand Label ), BUFLOMEDIL ...

During the same period patient was treated with IRBESARTAN (View Irbesartan Side Effects and Irbesartan Label ), BUFLOMEDIL (View Buflomedil Side Effects and Buflomedil Label ...

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Buflomedil Reactions
Bradycardia
Clonus
Haematoma
Hip Fracture
Hypotension
Prothrombin Level Decreased
Renal Failure Acute
Thrombocytopenia
Tremor
Buflomedil 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 Buflomedil 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!