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Danazol adverse events reported to FDA.

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Summary

FDA Adverse Reports: 14. View All

Danazol FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 8

Danazol Dosage, Warnings, Usage.

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

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6859962-5 | Off Label Use, Renal Failure Acute, Rhabdomyolysis
on Jun 09, 2010 Male patient from SERBIA , 80 years of age, weighting 198.4 lb, was diagnosed with idiopathic thrombocytopenic purpura and was treated with Danazol (View Usage). Patient experienced the following unwanted or unexpected effects: off label use, renal failure acute, rhabdomyolysis. Danazol dosage: . During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ). Patient was hospitalized.

6346883-X | Arrhythmia, Claustrophobia, Emotional Disorder, Fear, Libido Increased, Obsessive Thoughts, Obsessive-compulsive Disorder, Panic Attack, Paranoia
Patient was taking Danazol (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), claustrophobia, emotional disorder, fear, libido increased, obsessive thoughts, obsessive-compulsive disorder (What is obsessive-compulsive disorder?), panic attack, paranoia on Sep 09, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 145.0 lb, was diagnosed with premenstrual syndrome (What is premenstrual syndrome?) and. Danazol dosage: 50 Mg Twice Daily As Needed For Pms Po. During the same period patient was treated with BUPROPION HCL (View Bupropion Hcl Review and Bupropion Hcl Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

6016076-4 | Obliterative Bronchiolitis, Organising Pneumonia
Adverse event was reported on Dec 08, 2008 by a Male patient taking Danazol (View Usage) (Dosage: ) was diagnosed with idiopathic thrombocytopenic purpura and. Location: UNITED STATES , 64 years of age, After Danazol was administered, patient had the following side effects: obliterative bronchiolitis, organising pneumonia. Patient was hospitalized.

5933471-X | Abdominal Discomfort, Abdominal Pain Lower, Blood Creatinine Increased, Cardiac Failure Congestive, Haemoglobin Decreased, Nausea, Oedema Peripheral, Rash
on Oct 20, 2008 Male patient from UNITED STATES , 70 years of age, weighting 209.9 lb, was diagnosed with paroxysmal nocturnal haemoglobinuria and was treated with Danazol (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, abdominal pain lower, blood creatinine increased, cardiac failure congestive, haemoglobin decreased, nausea (What is nausea?), oedema peripheral, rash (What is rash?). Danazol dosage: Oral. During the same period patient was treated with SOLIRIS (600 Mg, Weekly, Intravenous; 900 Mg, Intravenous) (View Soliris Review and Soliris Label ), EXJADE (500 Mg, Qid, Oral; 500 Mg, Tid, Oral) (View Exjade Review and Exjade Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.


5903150-3 | Amnesia, Convulsion, Loss Of Consciousness
on Sep 29, 2008 Female patient from UNITED STATES , 26 years of age, weighting 175.0 lb, was treated with Danazol (View Usage). Patient had the following side effects: amnesia, convulsion, loss of consciousness. Danazol dosage: . Patient was hospitalized and became disabled.

5852249-9 | Incorrect Dose Administered
Patient was taking Danazol (View Usage). After Danazol was administered, patient had the following side effects: incorrect dose administered on Aug 20, 2008 from UNITED STATES Additional patient health information: Female patient , 30 years of age, . Danazol dosage: Capsule.

5852198-6 | Incorrect Dose Administered
Adverse event was reported on Aug 20, 2008 by a Female patient taking Danazol (View Usage) (Dosage: Capsule) . Location: UNITED STATES , 30 years of age, Patient experienced the following unwanted or unexpected effects: incorrect dose administered.

5239750-6 | Blood Creatine Phosphokinase Increased, Chromaturia, Dyspnoea Exertional, Exercise Lack Of, Gait Disturbance, Liver Function Test Abnormal, Muscle Tightness, Muscular Weakness, Musculoskeletal Discomfort
on Feb 14, 2007 Female patient from UNITED STATES , 81 years of age, weighting 154.3 lb, was diagnosed with idiopathic thrombocytopenic purpura, hyperlipidaemia and was treated with Danazol (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, chromaturia, dyspnoea exertional, exercise lack of, gait disturbance, liver function test abnormal, muscle tightness, muscular weakness, musculoskeletal discomfort. Danazol dosage: 200mg Bid Po. During the same period patient was treated with SIMVASTATIN (80mg Daily Po) (View Simvastatin Review and Simvastatin Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), METOPROLOL SUCCINATE (View Metoprolol Succinate Review and Metoprolol Succinate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ). Patient was hospitalized.

5199628-3 | Alanine Aminotransferase Increased, Anaemia, Aspartate Aminotransferase Increased, Hyponatraemia
on Jan 02, 2007 Female patient from UNITED STATES , 86 years of age, weighting 150.0 lb, was diagnosed with anaemia haemolytic autoimmune and was treated with Danazol (View Usage). After Danazol was administered, patient had the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, hyponatraemia. Danazol dosage: 200 Mg Bid Po. During the same period patient was treated with SULFASALAZINE (View Sulfasalazine Review and Sulfasalazine Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), DORZOLAMIDE HCL (View Dorzolamide Hcl Review and Dorzolamide Hcl Label ), LATANOPROST OPTH. SUSP (View Latanoprost Opth. Susp Review and Latanoprost Opth. Susp Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ).

5176479-7 | Carotid Artery Dissection, Hemiparesis
Patient was taking Danazol (View Usage). Patient experienced the following unwanted or unexpected effects: carotid artery dissection, hemiparesis on Dec 05, 2006 from UNITED KINGDOM Additional patient health information: Female patient , 41 years of age, was diagnosed with menorrhagia, pain (What is pain?) and. Danazol dosage: . During the same period patient was treated with DIHYDROCODEINE BITARTRATE INJ (View Dihydrocodeine Bitartrate Inj Review and Dihydrocodeine Bitartrate Inj Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ). Patient was hospitalized and became disabled.

5005848-0 | Back Pain, Diabetes Mellitus, Fibromyalgia, Fluid Retention, Joint Lock, Joint Swelling, Muscle Spasms
Adverse event was reported on Apr 27, 2006 by a Female patient taking Danazol (View Usage) (Dosage: 1 Caps., Oral) was diagnosed with angioneurotic oedema and. Location: UNITED STATES , 65 years of age, weighting 169.8 lb, Patient had the following side effects: back pain (What is back pain?), diabetes mellitus, fibromyalgia, fluid retention, joint lock, joint swelling, muscle spasms. During the same period patient was treated with LANTUS (Subcutaneous) (View Lantus Review and Lantus Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), ALLEGRA (View Allegra Review and Allegra Label ).

4941839-3 | Priapism
on Mar 01, 2006 Male patient from UNITED KINGDOM , 42 years of age, was diagnosed with hereditary angioedema, headache (What is headache?) and was treated with Danazol (View Usage). After Danazol was administered, patient had the following side effects: priapism. Danazol dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ).

4613580-8 | Cardiomyopathy, Condition Aggravated, Ejection Fraction Decreased, Pulmonary Oedema, Rheumatoid Arthritis
on Mar 01, 2005 Female patient from , 66 years of age, was treated with Danazol (View Usage). Patient experienced the following unwanted or unexpected effects: cardiomyopathy (What is cardiomyopathy?), condition aggravated, ejection fraction decreased, pulmonary oedema, rheumatoid arthritis (What is rheumatoid arthritis?). Danazol dosage: 200 Mg Bid; Oral. During the same period patient was treated with DECAPEPTYL NOVUM SLOW RELEASE (TRIPTORELIN EMBONATE) SOLUTION (0.1 Mg 1/month; Subcutaneous) (View Decapeptyl Novum - Slow Release - (triptorelin Embonate) - Solution - Review and Decapeptyl Novum - Slow Release - (triptorelin Embonate) - Solution - Label ), BIOCARDE (AUBEPINE/VALERIANA/MELISSA/PASIFLORA/AGRIPALMA/AVENA) SL (View Biocarde - (aubepine/valeriana/melissa/pasiflora/agripalma/avena) - Sl Review and Biocarde - (aubepine/valeriana/melissa/pasiflora/agripalma/avena) - Sl Label ), PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

4603148-1 | Alveolitis Allergic, Hypoxia, Pulmonary Toxicity
Patient was taking Danazol (View Usage). Patient had the following side effects: alveolitis allergic, hypoxia, pulmonary toxicity on Oct 17, 2005 from Additional patient health information: Male patient , 65 years of age, was diagnosed with refractory anaemia with an excess of blasts and. Danazol dosage: 600 Mg Qd; Oral. 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 Danazol 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 Danazol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Danazol 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 DANAZOL (View Danazol Review and Danazol Label ). Patient was hospitalized. 5517960-8 | Embolic Cerebral Infarction<<<<

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Danazol Reactions
Abdominal Discomfort
Abdominal Pain Lower
Alanine Aminotransferase Increased
Alveolitis Allergic
Amnesia
Anaemia
ArrhythmiaWhat is Arrhythmia?
Aspartate Aminotransferase Increased
Back PainWhat is Back pain?
Blood Creatine Phosphokinase Increased
Blood Creatinine Increased
Cardiac Failure Congestive
CardiomyopathyWhat is Cardiomyopathy?
Carotid Artery Dissection
Chromaturia
Claustrophobia
Condition Aggravated
Convulsion
Diabetes Mellitus
Dyspnoea Exertional
Ejection Fraction Decreased
Emotional Disorder
Exercise Lack Of
Fear
Fibromyalgia
Fluid Retention
Gait Disturbance
Haemoglobin Decreased
Hemiparesis
Incorrect Dose Administered
Danazol 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 Danazol 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!