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Danatrol adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Danatrol FDA safety alerts: No

Reported hospitalizations: 7

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

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6689814-5 | Cytolytic Hepatitis, Diabetes Mellitus
on Apr 14, 2010 Male patient from FRANCE , 64 years of age, was diagnosed with myelofibrosis, splenomegaly and was treated with Danatrol (View Usage). Patient experienced the following unwanted or unexpected effects: cytolytic hepatitis, diabetes mellitus. Danatrol dosage: . During the same period patient was treated with VERCYTE (View Vercyte Review and Vercyte Label ). Patient was hospitalized.

5823356-1 | Chest Pain
Patient was taking Danatrol (View Usage). Patient had the following side effects: chest pain (What is chest pain?) on Jul 27, 2007 from FRANCE Additional patient health information: Female patient , 87 years of age, . Danatrol dosage: Unk. Patient was hospitalized.

5412667-X | Demyelination, Weight Increased
Adverse event was reported on Aug 07, 2007 by a Female patient taking Danatrol (View Usage) (Dosage: Unk) was diagnosed with endometriosis (What is endometriosis?) and. Location: BELGIUM , weighting 262.4 lb, After Danatrol was administered, patient had the following side effects: demyelination, weight increased.

5408575-0 | Chest Pain
on Jul 27, 2007 Female patient from FRANCE , 87 years of age, was treated with Danatrol (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?). Danatrol dosage: Unk. Patient was hospitalized.


5390320-9 | Oestradiol Increased, Ovarian Hyperfunction
on Jul 11, 2007 Female patient from SWITZERLAND , 49 years of age, was diagnosed with aplastic anaemia and was treated with Danatrol (View Usage). Patient had the following side effects: oestradiol increased, ovarian hyperfunction. Danatrol dosage: .

4973526-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Asthenia, Blood Creatine Phosphokinase Increased, Muscular Weakness, Pain In Extremity
Patient was taking Danatrol (View Usage). After Danatrol was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, asthenia, blood creatine phosphokinase increased, muscular weakness, pain in extremity on Feb 28, 2006 from FRANCE Additional patient health information: Male patient , weighting 167.6 lb, was diagnosed with thrombocytopenia and. Danatrol dosage: . During the same period patient was treated with CORTANCYL (80 Mg) (View Cortancyl Review and Cortancyl Label ), ZOCOR (Unk) (View Zocor Review and Zocor Label ), EUPANTOL (Unk) (View Eupantol Review and Eupantol Label ), COVERSYL (View Coversyl Review and Coversyl Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ZANIDIP (View Zanidip Review and Zanidip Label ).

4787482-0 | Fluid Retention, Oedema Peripheral, Orthopnoea, Pleural Effusion, Sodium Retention, Weight Increased
Adverse event was reported on Aug 11, 2005 by a Male patient taking Danatrol (View Usage) (Dosage: ) was diagnosed with idiopathic thrombocytopenic purpura and. Location: FRANCE , 57 years of age, weighting 249.1 lb, Patient experienced the following unwanted or unexpected effects: fluid retention, oedema peripheral, orthopnoea, pleural effusion, sodium retention, weight increased. During the same period patient was treated with TENORDATE (View Tenordate Review and Tenordate Label ), INSULIN (View Insulin Review and Insulin Label ), TAHOR (View Tahor Review and Tahor Label ), DIFFU K (View Diffu K Review and Diffu K Label ), TARDYFERON (3 Unit) (View Tardyferon Review and Tardyferon Label ). Patient was hospitalized.

4750563-1 | Asthenia, Blood Lactate Dehydrogenase Increased, Cardiomegaly, Creatinine Renal Clearance Increased, Fluid Retention, Mitral Valve Incompetence, Oedema Peripheral, Orthopnoea, Pleural Effusion
on Aug 11, 2005 Male patient from FRANCE , 57 years of age, weighting 249.1 lb, was diagnosed with idiopathic thrombocytopenic purpura and was treated with Danatrol (View Usage). Patient had the following side effects: asthenia, blood lactate dehydrogenase increased, cardiomegaly, creatinine renal clearance increased, fluid retention, mitral valve incompetence, oedema peripheral, orthopnoea, pleural effusion. Danatrol dosage: . During the same period patient was treated with TENORDATE (View Tenordate Review and Tenordate Label ), INSULIN (View Insulin Review and Insulin Label ), TAHOR (View Tahor Review and Tahor Label ), LASIX (View Lasix Review and Lasix Label ), DIFFU K (View Diffu K Review and Diffu K Label ), TARDYFERON (3 Unit) (View Tardyferon Review and Tardyferon Label ). Patient was hospitalized.

4608762-5 | Dermatitis Exfoliative, Toxic Skin Eruption
on Mar 03, 2005 Male patient from , 89 years of age, was diagnosed with idiopathic thrombocytopenic purpura and was treated with Danatrol (View Usage). After Danatrol was administered, patient had the following side effects: dermatitis exfoliative, toxic skin eruption. Danatrol dosage: 600 Mg. During the same period patient was treated with POLYKARAYA (12 G) (View Polykaraya Review and Polykaraya Label ), DIFFU K (1800 Mg) (View Diffu K Review and Diffu K Label ), RABEPRAZOLE SODIUM (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ), DIAFUSOR (View Diafusor Review and Diafusor Label ). Patient was hospitalized.

4605187-3 | Cardiomyopathy, Pulmonary Oedema
Patient was taking Danatrol (View Usage). Patient experienced the following unwanted or unexpected effects: cardiomyopathy (What is cardiomyopathy?), pulmonary oedema on Mar 01, 2005 from Additional patient health information: Female patient , 66 years of age, . Danatrol dosage: . During the same period patient was treated with DECAPEPTYL (View Decapeptyl Review and Decapeptyl Label ), CONTRAMAL (View Contramal Review and Contramal Label ), ENDOXAN (View Endoxan Review and Endoxan Label ), BIOCARDE (View Biocarde Review and Biocarde Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ). Patient was hospitalized.


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Danatrol Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

STELLA   ATHENS

12:25pm on Saturday, October 30th, 2010

I HAVE ENDOMETRIOSIS AND TODAY I STOPPED THE THERAPY WITH DANATROL PILLS. WHEN CAN I TRY FOR PREGNA... read more »

andreas tzatzimos   Athens

3:03am on Tuesday, January 12th, 2010

can i take danatrol with kepra?

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 Danatrol 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 Danatrol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Danatrol 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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Danatrol Reactions
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Asthenia
Blood Creatine Phosphokinase Increased
Blood Lactate Dehydrogenase Increased
Cardiomegaly
CardiomyopathyWhat is Cardiomyopathy?
Chest PainWhat is Chest pain?
Creatinine Renal Clearance Increased
Cytolytic Hepatitis
Demyelination
Dermatitis Exfoliative
Diabetes Mellitus
Fluid Retention
Mitral Valve Incompetence
Muscular Weakness
Oedema Peripheral
Oestradiol Increased
Orthopnoea
Ovarian Hyperfunction
Pain In Extremity
Pleural Effusion
Pulmonary Oedema
Sodium Retention
Toxic Skin Eruption
Weight Increased
Danatrol 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 Danatrol 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!