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Dantrolene adverse events reported to FDA.

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Summary

FDA Adverse Reports: 1. View All

Dantrolene FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 3

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

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4553830-X | Hepatotoxicity, Liver Function Test Abnormal
on Jan 10, 2005 Female patient from , 54 years of age, weighting 198.0 lb, was diagnosed with neuroleptic malignant syndrome and was treated with Dantrolene (View Usage). Patient experienced the following unwanted or unexpected effects: hepatotoxicity, liver function test abnormal. Dantrolene dosage: 25 Mg Q 6 Hrs- Tolrate- Upward To 50 Mg Q6 Hr. During the same period patient was treated with CYANOCOBALAMIN (View Cyanocobalamin Review and Cyanocobalamin Label ), ENOXAPARIN SODIUM (View Enoxaparin Sodium Review and Enoxaparin Sodium Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), INSULIN ASPARTAMINE (View Insulin Aspartamine Review and Insulin Aspartamine Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), POTASSIUM (View Potassium Review and Potassium Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ).


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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 Dantrolene 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 Dantrolene quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Dantrolene 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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During the same period patient was treated with DANTRIUM (DANTROLENE SODIUM) (NR) (25 Mg (nr) Po) (View Dantrium (dantrolene Sodium) (nr) Review and Dantrium (dantrolene ...

During the same period patient was treated with DANTRIUM (DANTROLENE SODIUM) (NR) (25 Mg (nr) Po) (View Dantrium (dantrolene Sodium) (nr) Review and Dantrium ...

... Valproate Sodium Review and Valproate Sodium Label ), BACLOFEN (40 Mg/day) (View Baclofen Review and Baclofen Label ), DANTROLENE (View Dantrolene Review and Dantrolene Label ).

During the same period patient was treated with DANTRIUM (DANTROLENE SODIUM) (NR) (25 Mg (nr) Po) (View Dantrium (dantrolene Sodium) (nr) Review and Dantrium (dantrolene ...

... off-label medications include glucocorticoids (deflazacort, prednisolone), (suxomethonium chloride, mexiletine, phenytoin, carbazepine), calcium antagonists (dantrolene ...

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

During the same period patient was treated with DANTROLENE SODIUM (View Dantrolene Sodium Review and Dantrolene Sodium Label ), ZANTAC (View Zantac Review and Zantac Label ...

... Baclofen Review and Baclofen Label ), TIZANIDINE HCL (View Tizanidine Hcl Review and Tizanidine Hcl Label ), DANTROLENE SODIUM (View Dantrolene Sodium Review and Dantrolene ...

(Consult dantrolene sodium intravenous package insert before using.) The following conditions may preclude the use of spinal anesthesia, depending upon the physicianâ ...

During the same period patient was treated with CARBAMAZEPINE (View Carbamazepine Review and Carbamazepine Label ), DANTROLENE (View Dantrolene Review and Dantrolene Label ).

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Dantrolene 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 Dantrolene 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!