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Summary

FDA Adverse Reports: 226. View All

Lanoxin FDA safety alerts: No

Reported deaths: 45

Reported hospitalizations: 100

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1Dear Sir, I Am Worried About Possible Renal Failure Due To My Daily Usage Of Lanoxin.25mg, What Are The Real Risks Of Long Time Usage I Would Like To Know, Currently Due To The Scare I Am Only Using Half The Tablet. Please Send Me Answer To My Email Id Shriram_kv@hotmail.com .Thanks.K.V.Shriram
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Often additional risks of using a medication, such as Lanoxin, 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 Lanoxin users, Learn more about unwanted side effects & find ways to reduce them. Browse Lanoxin Adverse Reports reported to FDA and participate in Lanoxin discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Lanoxin. 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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Lanoxin Adverse Effect Reports (FDA)

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6937727-3 | Agitation, Dizziness, Hypoaesthesia Facial, Nasal Congestion, Product Substitution Issue, Swelling Face
on Aug 20, 2010 Female patient from UNITED STATES , 49 years of age, was diagnosed with cardiac failure congestive, cardiomyopathy (What is cardiomyopathy?) and was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: agitation, dizziness (What is dizziness?), hypoaesthesia facial, nasal congestion, product substitution issue, swelling face. Lanoxin dosage: 125 Mcg. Once Daily Oral. During the same period patient was treated with COREG (View Coreg Review and Coreg Label ), ZESTRIL (View Zestril Review and Zestril Label ), LASIX (View Lasix Review and Lasix Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ).

6896256-6 | Convulsion, Myocardial Infarction
Patient was taking Lanoxin (View Usage). Patient had the following side effects: convulsion, myocardial infarction on Jul 30, 2010 from UNITED STATES Additional patient health information: Male patient , 58 years of age, . Lanoxin dosage: .25mg Per Day. During the same period patient was treated with BLOOD THINNER (View Blood Thinner Review and Blood Thinner Label ).

6769936-0 |
Adverse event was reported on Jun 07, 2010 by a Female patient taking Lanoxin (View Usage) (Dosage: ) . Location: UNITED STATES , 67 years of age, . During the same period patient was treated with COREG (View Coreg Review and Coreg Label ).

6737601-1 | Cardiogenic Shock, Continuous Haemodiafiltration, Disorientation, Electrocardiogram Qrs Complex Prolonged, Electrocardiogram Qt Prolonged, Renal Failure, Ventricular Arrhythmia
on May 10, 2010 Male patient from NETHERLANDS , 75 years of age, was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: cardiogenic shock, continuous haemodiafiltration, disorientation, electrocardiogram qrs complex prolonged, electrocardiogram qt prolonged, renal failure, ventricular arrhythmia. Lanoxin dosage: . During the same period patient was treated with SOTALOL HCL (View Sotalol Hcl Review and Sotalol Hcl Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ). Patient was hospitalized.


6719757-X | Fall, Influenza, Limb Injury, Pneumonia
on May 04, 2010 Female patient from UNITED STATES , 81 years of age, was treated with Lanoxin (View Usage). Patient had the following side effects: fall (What is fall?), influenza, limb injury, pneumonia (What is pneumonia?). Lanoxin dosage: .0125mg Per Day. During the same period patient was treated with OXYGEN (View Oxygen Review and Oxygen Label ), ARICEPT (View Aricept Review and Aricept Label ), NAMENDA (View Namenda Review and Namenda Label ), SPIRIVA (View Spiriva Review and Spiriva Label ). Patient was hospitalized.

6704997-6 | Cardiac Failure Congestive, Deafness, Ear Pain, Heart Valve Incompetence, Hypotension
Patient was taking Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: cardiac failure congestive, deafness, ear pain, heart valve incompetence, hypotension on Apr 22, 2010 from UNITED STATES Additional patient health information: Female patient , 76 years of age, was diagnosed with pulmonary hypertension (What is pulmonary hypertension?) and. Lanoxin dosage: . During the same period patient was treated with REVATIO (20mg Three Times Per Day) (View Revatio Review and Revatio Label ), TRACLEER (View Tracleer Review and Tracleer Label ), OXYGEN (View Oxygen Review and Oxygen Label ), PROAIR HFA (View Proair Hfa Review and Proair Hfa Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), DEMADEX (View Demadex Review and Demadex Label ), COREG (View Coreg Review and Coreg Label ), KLONOPIN (View Klonopin Review and Klonopin Label ).

6640974-1 | Renal Failure, Therapeutic Agent Toxicity
Adverse event was reported on Mar 08, 2010 by a Male patient taking Lanoxin (View Usage) (Dosage: .25mg Per Day) . Location: UNITED STATES , 70 years of age, weighting 357.1 lb, Patient experienced the following unwanted or unexpected effects: renal failure, therapeutic agent toxicity. Patient was hospitalized.

6575597-6 | Renal Failure, Therapeutic Agent Toxicity
on Feb 03, 2010 Male patient from UNITED STATES , 70 years of age, was treated with Lanoxin (View Usage). Patient had the following side effects: renal failure, therapeutic agent toxicity. Lanoxin dosage: 2.5mg Per Day. Patient was hospitalized.

6534584-4 | Dyskinesia, Feeling Abnormal, Hallucination, Social Avoidant Behaviour, Visual Impairment
on Jan 08, 2010 Female patient from UNITED STATES , 97 years of age, was diagnosed with cardiac failure, change of bowel habit and was treated with Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: dyskinesia, feeling abnormal, hallucination, social avoidant behaviour, visual impairment. Lanoxin dosage: .5tab Per Day. During the same period patient was treated with METOPROLOL (View Metoprolol Review and Metoprolol Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), POTASSIUM (View Potassium Review and Potassium Label ), OSTEOBIFLEX (View Osteobiflex Review and Osteobiflex Label ), LASIX (View Lasix Review and Lasix Label ), AMITIZA (View Amitiza Review and Amitiza Label ), CALCIUM (View Calcium Review and Calcium Label ).

6533323-0 | Adverse Event, Neoplasm Malignant
Patient was taking Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: adverse event, neoplasm malignant on Jan 07, 2010 from UNITED STATES Additional patient health information: Female patient , 83 years of age, was diagnosed with cardiac failure, herpes simplex (What is herpes simplex?) and. Lanoxin dosage: .25mg Per Day. During the same period patient was treated with ZOVIRAX (400mg As Required) (View Zovirax Review and Zovirax Label ), NEXIUM (View Nexium Review and Nexium Label ), ZETIA (View Zetia Review and Zetia Label ), PLAVIX (View Plavix Review and Plavix Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ). Patient was hospitalized.

6522292-5 | Electrocardiogram St Segment Abnormal, Therapeutic Agent Toxicity
Adverse event was reported on Dec 23, 2009 by a Female patient taking Lanoxin (View Usage) (Dosage: ) . Location: UNITED STATES , 90 years of age, Patient had the following side effects: electrocardiogram st segment abnormal, therapeutic agent toxicity. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), LASIX (View Lasix Review and Lasix Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

6490716-8 | Accidental Overdose, Bradycardia
on Dec 02, 2009 Male patient from BELGIUM , weighting 9.48 lb, was diagnosed with atrial flutter and was treated with Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: accidental overdose, bradycardia. Lanoxin dosage: 180mcg Four Times Per Day. During the same period patient was treated with NUTRAMIGEN (View Nutramigen Review and Nutramigen Label ), LOSEC (4mg Twice Per Day) (View Losec Review and Losec Label ), MOTILIUM (View Motilium Review and Motilium Label ), PERFUSION (15ml See Dosage Text) (View Perfusion Review and Perfusion Label ), NEOBACITRACINE (2drop Three Times Per Day) (View Neobacitracine Review and Neobacitracine Label ). Patient was hospitalized.

6456673-5 | Arrhythmia, Middle Insomnia
on Jun 11, 2009 Male patient from UNITED STATES , 81 years of age, was diagnosed with arrhythmia (What is arrhythmia?) and was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: arrhythmia (What is arrhythmia?), middle insomnia. Lanoxin dosage: .125mg Per Day. During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), LOVASTATIN (View Lovastatin Review and Lovastatin Label ).

6456671-1 | Blood Glucose Abnormal, Blood Glucose Increased
Patient was taking Lanoxin (View Usage). Patient had the following side effects: blood glucose abnormal, blood glucose increased on Mar 27, 2009 from UNITED STATES Additional patient health information: Male patient , 70 years of age, was diagnosed with prostate cancer (What is prostate cancer?) and. Lanoxin dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), LEUPROLIDE ACETATE (22.5mg See Dosage Text) (View Leuprolide Acetate Review and Leuprolide Acetate Label ), DOCETAXEL (View Docetaxel Review and Docetaxel Label ), LEVOTHYROXINE (View Levothyroxine Review and Levothyroxine Label ), ZOLEDRONIC ACID (View Zoledronic Acid Review and Zoledronic Acid Label ), PEGFILGRASTIM (View Pegfilgrastim Review and Pegfilgrastim Label ), CALCIUM (View Calcium Review and Calcium Label ), MAGNESIUM (View Magnesium Review and Magnesium Label ).

6456670-X | Heart Rate Increased, Insomnia
Adverse event was reported on Mar 06, 2009 by a Female patient taking Lanoxin (View Usage) (Dosage: .19mg Per Day) was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Location: UNITED STATES , 87 years of age, After Lanoxin was administered, patient had the following side effects: heart rate increased, insomnia. During the same period patient was treated with NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), COZAAR (View Cozaar Review and Cozaar Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ).

6456668-1 | Heart Rate Irregular, Hypertension
on Feb 04, 2009 Female patient from UNITED STATES , 75 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: heart rate irregular, hypertension. Lanoxin dosage: .375mcg Per Day. During the same period patient was treated with VERAPAMIL (View Verapamil Review and Verapamil Label ), ATROMID S 500 (View Atromid-s 500 Review and Atromid-s 500 Label ), LIPITOR (View Lipitor Review and Lipitor Label ), METFORMIN (View Metformin Review and Metformin Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6456665-6 | Hallucination, Nausea, Product Quality Issue
on Jan 28, 2009 Female patient from UNITED STATES , 89 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). Patient had the following side effects: hallucination, nausea (What is nausea?), product quality issue. Lanoxin dosage: .125mg Per Day. During the same period patient was treated with DILTIAZEM (View Diltiazem Review and Diltiazem Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), GLUCOTROL (View Glucotrol Review and Glucotrol Label ), JANUVIA (View Januvia Review and Januvia Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), SINGULAIR (View Singulair Review and Singulair Label ).

6456664-4 | Feeling Abnormal, Halo Vision, Product Quality Issue
Patient was taking Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: feeling abnormal, halo vision, product quality issue on Dec 04, 2008 from UNITED STATES Additional patient health information: Female patient , 36 years of age, . Lanoxin dosage: 250mcg Twice Per Day. During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), LANOXICAPS (View Lanoxicaps Review and Lanoxicaps Label ).

6456663-2 | Depression, Diarrhoea, Immobile, Mental Impairment, Mood Altered, Nausea, Swelling Face
Adverse event was reported on Feb 18, 2009 by a Female patient taking Lanoxin (View Usage) (Dosage: ) was diagnosed with cardiac failure and. Location: UNITED STATES , 36 years of age, Patient experienced the following unwanted or unexpected effects: depression (What is depression?), diarrhoea, immobile, mental impairment, mood altered, nausea (What is nausea?), swelling face. During the same period patient was treated with LANOXICAPS (View Lanoxicaps Review and Lanoxicaps Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), ZESTRIL (10mg Per Day) (View Zestril Review and Zestril Label ), COREG (View Coreg Review and Coreg Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), KLONOPIN (View Klonopin Review and Klonopin Label ).

6456662-0 | Asthenia, Cardiac Disorder, Chest Discomfort, Dizziness, Dyspnoea, Dyspnoea At Rest, Headache, Muscular Weakness, Speech Disorder
on Oct 20, 2008 Female patient from UNITED STATES , 61 years of age, was treated with Lanoxin (View Usage). Patient had the following side effects: asthenia, cardiac disorder, chest discomfort, dizziness (What is dizziness?), dyspnoea, dyspnoea at rest, headache (What is headache?), muscular weakness, speech disorder. Lanoxin dosage: .5tab Per Day. During the same period patient was treated with LOPRESSOR (View Lopressor Review and Lopressor Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), PREMARIN (View Premarin Review and Premarin Label ), PROVERA (View Provera Review and Provera Label ), QVAR 40 (View Qvar 40 Review and Qvar 40 Label ), ATIVAN (View Ativan Review and Ativan Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6456660-7 | Blood Potassium Increased, Heart Rate Irregular, Pollakiuria, Weight Decreased
on Mar 17, 2009 Male patient from UNITED STATES , 80 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: blood potassium increased, heart rate irregular, pollakiuria, weight decreased. Lanoxin dosage: .25mg Per Day. During the same period patient was treated with COZAAR (50mg Per Day) (View Cozaar Review and Cozaar Label ), MEVACOR (View Mevacor Review and Mevacor Label ).

6430538-7 | Atrial Fibrillation, Heart Rate Increased, Heart Rate Irregular
Patient was taking Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: atrial fibrillation (What is atrial fibrillation?), heart rate increased, heart rate irregular on Nov 02, 2009 from UNITED STATES Additional patient health information: Male patient , 81 years of age, was diagnosed with emphysema and. Lanoxin dosage: .125mg Per Day. During the same period patient was treated with FLOVENT (2puff Twice Per Day) (View Flovent Review and Flovent Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), XOPENEX (View Xopenex Review and Xopenex Label ), NEBULIZER (View Nebulizer Review and Nebulizer Label ), ONE A DAY (View One A Day Review and One A Day Label ), DIAVAN (View Diavan Review and Diavan Label ), FLECAINIDE ACETATE (View Flecainide Acetate Review and Flecainide Acetate Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

6408797-6 | Conjunctival Hyperaemia, Dysgraphia, Paraesthesia, Pruritus, Vision Blurred, Visual Impairment
Adverse event was reported on Oct 14, 2009 by a Male patient taking Lanoxin (View Usage) (Dosage: ) was diagnosed with heart disease congenital and. Location: BELGIUM , child 7 years of age, weighting 46.30 lb, Patient had the following side effects: conjunctival hyperaemia, dysgraphia, paraesthesia, pruritus, vision blurred, visual impairment. During the same period patient was treated with ASAFLOW (View Asaflow Review and Asaflow Label ), ZESTRIL (View Zestril Review and Zestril Label ).

6368984-2 | Asthenia, Blood Pressure Decreased, Brain Natriuretic Peptide Increased, Bronchitis, Dizziness, Dyspnoea, Electrocardiogram Abnormal, International Normalised Ratio Increased, Vomiting
on Sep 18, 2009 Female patient from UNITED STATES , 66 years of age, weighting 136.7 lb, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: asthenia, blood pressure decreased, brain natriuretic peptide increased, bronchitis (What is bronchitis?), dizziness (What is dizziness?), dyspnoea, electrocardiogram abnormal, international normalised ratio increased, vomiting. Lanoxin dosage: 0.25mg Daily Po. During the same period patient was treated with WARFARIN SODIUM (5mg Daily Po) (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

6288470-8 | Parkinson's Disease
on Jul 23, 2009 Female patient from NETHERLANDS , weighting 132.3 lb, was diagnosed with arrhythmia (What is arrhythmia?) and was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: parkinson's disease (What is parkinson's disease?). Lanoxin dosage: .0625mg Per Day. During the same period patient was treated with FUROSEMIDE (80mg Per Day) (View Furosemide Review and Furosemide Label ), SPIRONOLACTONE (50mg Per Day) (View Spironolactone Review and Spironolactone Label ), BISOPROLOL FUMARATE (1.25mg Per Day) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), AZILECT (1mg Per Day) (View Azilect Review and Azilect Label ), SINEMET (View Sinemet Review and Sinemet Label ), SIFROL (125mcg Per Day) (View Sifrol Review and Sifrol Label ).

6283901-1 | Arrhythmia
Patient was taking Lanoxin (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?) on Jul 22, 2009 from UNITED STATES Additional patient health information: Male patient , 54 years of age, weighting 199.0 lb, was diagnosed with hypertrophic cardiomyopathy and. Lanoxin dosage: 2 To 3 Tablets Daily Po.

6254659-7 | Dysgraphia, Visual Impairment
Adverse event was reported on Jun 25, 2009 by a Male patient taking Lanoxin (View Usage) (Dosage: ) was diagnosed with heart disease congenital and. Location: BELGIUM , child 7 years of age, After Lanoxin was administered, patient had the following side effects: dysgraphia, visual impairment.

6230725-7 | Dehydration, Influenza, Malaise, Product Measured Potency Issue
on Jun 11, 2009 Female patient from UNITED STATES , weighting 112.0 lb, was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: dehydration, influenza, malaise, product measured potency issue. Lanoxin dosage: 0.25 Mg (now) 1 Ea. Day By Mouth. Patient was hospitalized.

6216813-X | Anaemia, Coronary Artery Thrombosis, Tumour Haemorrhage
on Jun 03, 2009 Female patient from UNITED STATES , 90 years of age, weighting 110.0 lb, was diagnosed with atrial fibrillation (What is atrial fibrillation?), heart rate irregular and was treated with Lanoxin (View Usage). Patient had the following side effects: anaemia, coronary artery thrombosis, tumour haemorrhage. Lanoxin dosage: .125 Mg 1/day.

6190295-9 | Decreased Appetite, Headache
Patient was taking Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: decreased appetite, headache (What is headache?) on May 05, 2009 from UNITED STATES Additional patient health information: Male patient , 93 years of age, . Lanoxin dosage: .125mcg Per Day.

6165126-3 | Gait Disturbance, Hypersomnia, Muscular Weakness, Renal Tubular Necrosis
Adverse event was reported on Apr 21, 2009 by a Male patient taking Lanoxin (View Usage) (Dosage: One Daily Po) was diagnosed with arrhythmia (What is arrhythmia?), cardiac failure and. Location: UNITED STATES , weighting 225.0 lb, Patient experienced the following unwanted or unexpected effects: gait disturbance, hypersomnia, muscular weakness, renal tubular necrosis. During the same period patient was treated with DIGOXIN (One Every Other Day Po) (View Digoxin Review and Digoxin Label ). Patient was hospitalized.

6161765-4 | Decreased Appetite, Somnolence
on Apr 17, 2009 Female patient from UNITED STATES , 79 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). Patient had the following side effects: decreased appetite, somnolence. Lanoxin dosage: 1 Daily Po.

6124655-9 | Asthenia, Diarrhoea, Malaise, Vertigo
on Mar 12, 2009 Female patient from ITALY , 79 years of age, was diagnosed with cardiac failure and was treated with Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: asthenia, diarrhoea, malaise, vertigo. Lanoxin dosage: .0625mg Twice Per Day. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), HYDROQUINIDINE (View Hydroquinidine Review and Hydroquinidine Label ), ENAPREN (20mg Twice Per Day) (View Enapren Review and Enapren Label ), KADIUR (View Kadiur Review and Kadiur Label ), CARDURA (4mg Twice Per Day) (View Cardura Review and Cardura Label ).

6119575-X | Agitation, Confusional State, Overdose
Patient was taking Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: agitation, confusional state, overdose on Mar 10, 2009 from ITALY Additional patient health information: Female patient , 64 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Lanoxin dosage: .25mg Per Day. During the same period patient was treated with ATENOLOL (100mg Per Day) (View Atenolol Review and Atenolol Label ), COUMADIN (View Coumadin Review and Coumadin Label ), TRIATEC (View Triatec Review and Triatec Label ), EUTIROX (View Eutirox Review and Eutirox Label ), SELEPARINA (View Seleparina Review and Seleparina Label ), LASIX (View Lasix Review and Lasix Label ).

6107170-8 | Balance Disorder, Chest Pain, Dizziness
Adverse event was reported on Mar 05, 2009 by a Male patient taking Lanoxin (View Usage) (Dosage: 1 Tablet Dailey Mouth) was diagnosed with neoplasm malignant, palpitations and. Location: UNITED STATES , weighting 225.0 lb, Patient had the following side effects: balance disorder, chest pain (What is chest pain?), dizziness (What is dizziness?). Patient was hospitalized.

6098880-X | Hypokalaemia
on Feb 25, 2009 Female patient from MALAYSIA , 84 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: hypokalaemia. Lanoxin dosage: .

6093933-4 | Abdominal Pain Upper, Asthenia, Blood Creatinine Increased, Cerebrovascular Accident, Disorientation, Dysphonia, Hallucination
on Feb 24, 2009 Male patient from UNITED STATES , 84 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, asthenia, blood creatinine increased, cerebrovascular accident, disorientation, dysphonia, hallucination. Lanoxin dosage: 25mg Per Day. During the same period patient was treated with AGGRENOX (View Aggrenox Review and Aggrenox Label ), NORVASC (View Norvasc Review and Norvasc Label ), AMILORIDE HCL AND HYDROCHLOROTHIAZIDE (View Amiloride Hcl And Hydrochlorothiazide Review and Amiloride Hcl And Hydrochlorothiazide Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6087301-9 |
Patient was taking Lanoxin (View Usage). on Feb 17, 2009 from UNITED STATES Additional patient health information: Female patient , 73 years of age, weighting 193.3 lb, . Lanoxin dosage: .

6082187-0 | Asthenia, Blood Creatinine Increased, Cerebrovascular Accident, Disorientation, Infection, Insomnia, Septic Shock, Speech Disorder
Adverse event was reported on Feb 16, 2009 by a Male patient taking Lanoxin (View Usage) (Dosage: 25mg Per Day) was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Location: UNITED STATES , 84 years of age, After Lanoxin was administered, patient had the following side effects: asthenia, blood creatinine increased, cerebrovascular accident, disorientation, infection (What is infection?), insomnia, septic shock, speech disorder. During the same period patient was treated with AGGRENOX (View Aggrenox Review and Aggrenox Label ), NORVASC (View Norvasc Review and Norvasc Label ), AMILORIDE HCL AND HYDROCHLOROTHIAZIDE (View Amiloride Hcl And Hydrochlorothiazide Review and Amiloride Hcl And Hydrochlorothiazide Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6077350-9 | Angioedema, Oedema Mucosal
on Feb 06, 2009 Male patient from NETHERLANDS , 56 years of age, weighting 176.4 lb, was diagnosed with sinusitis (What is sinusitis?), atrial fibrillation (What is atrial fibrillation?) and was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, oedema mucosal. Lanoxin dosage: . During the same period patient was treated with AMOXICILLIN AND CLAVULANATE POTASSIUM (View Amoxicillin And Clavulanate Potassium Review and Amoxicillin And Clavulanate Potassium Label ), SELOKEEN ZOC (25mg Per Day) (View Selokeen Zoc Review and Selokeen Zoc Label ), FENPROCOUMON (View Fenprocoumon Review and Fenprocoumon Label ), NASONEX (50mcg Per Day) (View Nasonex Review and Nasonex Label ), DOXYCYCLINE (View Doxycycline Review and Doxycycline Label ).

6077313-3 | Bronchopneumonia
on Feb 05, 2009 Male patient from IRELAND , 70 years of age, was treated with Lanoxin (View Usage). Patient had the following side effects: bronchopneumonia. Lanoxin dosage: . During the same period patient was treated with HYDROMORPHONE HCL (View Hydromorphone Hcl Review and Hydromorphone Hcl Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ). Patient was hospitalized.

6077286-3 | Anaemia, Asthenia, Dizziness, Product Quality Issue
Patient was taking Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: anaemia, asthenia, dizziness (What is dizziness?), product quality issue on Feb 09, 2009 from UNITED STATES Additional patient health information: Female patient , 83 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Lanoxin dosage: .125mg Per Day. During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), METOLAZONE (View Metolazone Review and Metolazone Label ).

6062974-5 |
Adverse event was reported on Jan 28, 2009 by a Male patient taking Lanoxin (View Usage) (Dosage: ) . Location: IRELAND , 70 years of age, . Patient was hospitalized.

6045548-1 | Arrhythmia, Atrial Fibrillation, Blood Potassium Increased, Blood Urea Increased, Bradycardia, Chest Pain, Contusion, Dizziness
on Jan 14, 2009 Female patient from PORTUGAL , 70 years of age, was treated with Lanoxin (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), atrial fibrillation (What is atrial fibrillation?), blood potassium increased, blood urea increased, bradycardia, chest pain (What is chest pain?), contusion, dizziness (What is dizziness?). Lanoxin dosage: .125mg Per Day. During the same period patient was treated with PROPRANOLOL (10mg Per Day) (View Propranolol Review and Propranolol Label ), QUINAPRIL HYDROCHLORIDE (View Quinapril Hydrochloride Review and Quinapril Hydrochloride Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ). Patient was hospitalized.

6035936-1 | Acute Pulmonary Oedema, Bacteria Urine Identified, Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Potassium Increased, Blood Urea Increased, C-reactive Protein Increased, Cardiac Failure, Cardiac Failure Congestive
on Jan 08, 2009 Female patient from PORTUGAL , 88 years of age, was treated with Lanoxin (View Usage). After Lanoxin was administered, patient had the following side effects: acute pulmonary oedema, bacteria urine identified, blood creatinine increased, blood lactate dehydrogenase increased, blood potassium increased, blood urea increased, c-reactive protein increased, cardiac failure, cardiac failure congestive. Lanoxin dosage: .125mg Per Day. During the same period patient was treated with VALSARTAN+HYDROCHLOROTHIAZIDE (View Valsartan+hydrochlorothiazide Review and Valsartan+hydrochlorothiazide Label ), ISOSORBIDE MONONITRATE (60mg Per Day) (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), TICLOPIDINE HYDROCHLORIDE (View Ticlopidine Hydrochloride Review and Ticlopidine Hydrochloride Label ), LANSOPRAZOLE (30mg Per Day) (View Lansoprazole Review and Lansoprazole Label ), ANTIDEPRESSANTS (View Antidepressants Review and Antidepressants Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ). Patient was hospitalized.

6035925-7 |
Patient was taking Lanoxin (View Usage). on Jan 06, 2009 from IRELAND Additional patient health information: Male patient , 70 years of age, . Lanoxin dosage: . Patient was hospitalized.

6031683-0 | Abasia, Alopecia, Blood Glucose Decreased, Dizziness, Night Sweats, Therapeutic Agent Toxicity
Adverse event was reported on Jan 05, 2009 by a Female patient taking Lanoxin (View Usage) (Dosage: ) was diagnosed with diabetes mellitus and. Location: UNITED STATES , 80 years of age, Patient had the following side effects: abasia, alopecia, blood glucose decreased, dizziness (What is dizziness?), night sweats, therapeutic agent toxicity. During the same period patient was treated with GLARGINE (30unit Per Day) (View Glargine Review and Glargine Label ). Patient was hospitalized.

6029970-5 |
on Jan 06, 2009 Male patient from IRELAND , 70 years of age, was treated with Lanoxin (View Usage). . Lanoxin dosage: . Patient was hospitalized.

6027364-X | Bradycardia, Cardiac Failure Congestive
on Dec 23, 2008 Female patient from PORTUGAL , 64 years of age, was treated with Lanoxin (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, cardiac failure congestive. Lanoxin dosage: . During the same period patient was treated with AMIODARONE HYDROCHLORIDE (200mg Per Day) (View Amiodarone Hydrochloride Review and Amiodarone Hydrochloride Label ), NEBIVOLOL HCL (View Nebivolol Hcl Review and Nebivolol Hcl Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), ESCITALOPRAM (View Escitalopram Review and Escitalopram Label ), CLOXAZOLAM (View Cloxazolam Review and Cloxazolam Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), LEVOTHYROXINE SODIUM (.1mg Per Day) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ). Patient was hospitalized.

5961037-4 | Abdominal Pain Upper, Diarrhoea
Patient was taking Lanoxin (View Usage). Patient had the following side effects: abdominal pain upper, diarrhoea on Aug 29, 2008 from UNITED STATES Additional patient health information: Female patient , 84 years of age, . Lanoxin dosage: .125mg Per Day. During the same period patient was treated with AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), DIAZEPAM (View Diazepam Review and Diazepam 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 Lanoxin 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 Lanoxin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lanoxin 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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Lanoxin Reactions
Abdominal Pain Upper
Anaemia
Anorexia
Asthenia
Atrial FibrillationWhat is Atrial fibrillation?
Blood Creatinine Increased
Blood Potassium Increased
Bradyarrhythmia
Bradycardia
Cardiac Failure Congestive
Chest PainWhat is Chest pain?
Completed Suicide
Confusional State
Death
Diarrhoea
Diplopia
DizzinessWhat is Dizziness?
Dyspnoea
Fatigue
Hallucination
HeadacheWhat is Headache?
Heart Rate Increased
Heart Rate Irregular
Hyperkalaemia
Hypotension
Malaise
NauseaWhat is Nausea?
Renal Failure
Therapeutic Agent Toxicity
Vomiting
Lanoxin 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 Lanoxin 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!