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Digitek Side Effects

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Common Digitek Side Effects


The most commonly reported Digitek side effects (click to view or check a box to report):

Dizziness (209)
Nausea (155)
Asthenia (104)
Fatigue (85)
Hypotension (77)
Vomiting (71)
Dyspnoea (63)
Diarrhoea (62)
Heart Rate Decreased (61)
Therapeutic Agent Toxicity (56)
Fall (48)
Anorexia (45)
Heart Rate Irregular (44)
Malaise (44)
Confusional State (44)
Cardiac Disorder (36)
Heart Rate Increased (32)
Vision Blurred (32)
Incorrect Dose Administered (27)
Feeling Abnormal (25)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Digitek Side Effects Reported to FDA



Digitek Side Effect Report#9159330
White Blood Cell Count Increased
This is a report of a 30-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: NA, who was treated with Digitek (dosage: NA, start time: 1998), combined with:
  • Enalapril
and developed a serious reaction and side effect(s): White Blood Cell Count Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Digitek treatment in female patients, resulting in White Blood Cell Count Increased side effect.
Digitek Side Effect Report#9159329
Red Blood Cell Count Decreased, Haemoglobin Decreased, Haematocrit Decreased, Monocyte Count Increased, Prothrombin Time Prolonged, Red Cell Distribution Width Increased
This report suggests a potential Digitek Red Blood Cell Count Decreased side effect(s) that can have serious consequences. A male patient (weight: NA) from US was diagnosed with the following symptoms/conditions: NA and used Digitek (dosage: NA) starting NS. After starting Digitek the patient began experiencing various side effects, including: Red Blood Cell Count Decreased, Haemoglobin Decreased, Haematocrit Decreased, Monocyte Count Increased, Prothrombin Time Prolonged, Red Cell Distribution Width IncreasedAdditional drugs used concurrently: NA. Although Digitek demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Red Blood Cell Count Decreased, may still occur.
Digitek Side Effect Report#6815137-7
Atrial Fibrillation, Cardiac Disorder, Cardiac Failure Congestive, Cardiogenic Shock, Coronary Artery Disease, Dizziness, Ejection Fraction Decreased, Fatigue, Incorrect Dose Administered
This Atrial Fibrillation problem was reported by a consumer or non-health professional from United States. A 45-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: atrial fibrillation. On
Jun 01, 2006 this consumer started treatment with Digitek .25 Mg Mylan (dosage: NA). The following drugs were being taken at the same time: NA. When using Digitek .25 Mg Mylan, the patient experienced the following unwanted symptoms/side effects: Atrial Fibrillation, Cardiac Disorder, Cardiac Failure Congestive, Cardiogenic Shock, Coronary Artery Disease, Dizziness, Ejection Fraction Decreased, Fatigue, Incorrect Dose AdministeredThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Atrial Fibrillation, may become evident only after a product is in use by the general population.
Digitek Side Effect Report#6438654-0
Anxiety, Benign Prostatic Hyperplasia, Blood Potassium Increased, Blood Pressure Increased, Cardiac Failure Congestive, Chronic Obstructive Pulmonary Disease, Diabetes Mellitus, Economic Problem, Hypertension
This Anxiety side effect was reported by a consumer or non-health professional from United States. A 73-year-old male patient (weight:NA) experienced the following symptoms/conditions: cardiac disorder.The patient was prescribed Digitek (drug dosage: 0.25 Mg; Qd; Po), which was initiated on NS. Concurrently used drugs:
  • K-dur
  • Lotrel
  • Aspirin
  • Singulair
  • Vytorin
  • Glucophage
  • Glucotrol
  • Lantus
.After starting to take Digitek the consumer reported adverse symptoms, such as: Anxiety, Benign Prostatic Hyperplasia, Blood Potassium Increased, Blood Pressure Increased, Cardiac Failure Congestive, Chronic Obstructive Pulmonary Disease, Diabetes Mellitus, Economic Problem, HypertensionThese side effects may potentially be related to Digitek. The patient was hospitalized.
Digitek Side Effect Report#6342147-9
Heart Rate Decreased, Product Quality Issue
This is a report of a female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: heart rate irregular, who was treated with Digitek 0.125 Bertek Pharmaceuticals (dosage: 1 Tablet Daily (filled 2/22/08; Original 10/15/07), start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Heart Rate Decreased, Product Quality Issue after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Digitek 0.125 Bertek Pharmaceuticals treatment in female patients, resulting in Heart Rate Decreased side effect. The patient was hospitalized and became disabled.
Digitek Side Effect Report#6217654-X
Abasia, Asthenia, Pain, Product Quality Issue
This report suggests a potential Digitek Actavis Totowa Llc. He Had Received A Prescription Of Digitek Abasia side effect(s) that can have serious consequences. A 86-year-old male patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: cardiac disorder and used Digitek Actavis Totowa Llc. He Had Received A Prescription Of Digitek (dosage: 250 Mcg 1 Time Daily Date Filled 9/27/2008) starting
Sep 27, 2008. After starting Digitek Actavis Totowa Llc. He Had Received A Prescription Of Digitek the patient began experiencing various side effects, including: Abasia, Asthenia, Pain, Product Quality IssueAdditional drugs used concurrently: NA.The patient was hospitalized. Although Digitek Actavis Totowa Llc. He Had Received A Prescription Of Digitek demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abasia, may still occur.
Digitek Side Effect Report#6163465-3
Atrial Fibrillation, Blood Pressure Decreased, Cardiac Disorder, Fatigue, Heart Rate Decreased, Product Quality Issue
This Atrial Fibrillation problem was reported by a consumer or non-health professional from United States. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: atrial fibrillation. On
Mar 12, 2009 this consumer started treatment with Digitek .125mg Bertek (dosage: 1 Daily Po). The following drugs were being taken at the same time:
  • Digoxin (1 Daily Po)
When using Digitek .125mg Bertek, the patient experienced the following unwanted symptoms/side effects: Atrial Fibrillation, Blood Pressure Decreased, Cardiac Disorder, Fatigue, Heart Rate Decreased, Product Quality IssueAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Atrial Fibrillation, may become evident only after a product is in use by the general population.
Digitek Side Effect Report#6133315-X
Blood Pressure Abnormal, Transient Ischaemic Attack
This Blood Pressure Abnormal side effect was reported by a consumer or non-health professional from United States. A 87-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Digitek 250mcg Received From Medco (drug dosage: Po), which was initiated on
Jan 01, 2007. Concurrently used drugs: NA..After starting to take Digitek 250mcg Received From Medco the consumer reported adverse symptoms, such as: Blood Pressure Abnormal, Transient Ischaemic AttackThese side effects may potentially be related to Digitek 250mcg Received From Medco. The patient was hospitalized.
Digitek Side Effect Report#6048312-2
Cardiac Arrest, Implantable Defibrillator Malfunction, No Therapeutic Response, Product Quality Issue
This is a report of a patient (weight: NA) from United States, suffering from the following health symptoms/conditions: cardiac failure congestive, who was treated with Digitek Amid Pharm./berteck Pharmaceutical (dosage: 125 Mcg Daily Po, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Cardiac Arrest, Implantable Defibrillator Malfunction, No Therapeutic Response, Product Quality Issue after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Digitek Amid Pharm./berteck Pharmaceutical treatment in patients, resulting in Cardiac Arrest side effect.
Digitek Side Effect Report#6034927-4
Cerebrovascular Accident, Heart Rate Irregular
This report suggests a potential Digitek .25mg Medco Cerebrovascular Accident side effect(s) that can have serious consequences. A 64-year-old male patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: NA and used Digitek .25mg Medco (dosage: NA) starting NS. After starting Digitek .25mg Medco the patient began experiencing various side effects, including: Cerebrovascular Accident, Heart Rate IrregularAdditional drugs used concurrently: NA.The patient was hospitalized. Although Digitek .25mg Medco demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cerebrovascular Accident, may still occur.
Digitek Side Effect Report#6010460-0
Cardiac Failure Congestive, Condition Aggravated, Therapeutic Agent Toxicity
This Cardiac Failure Congestive problem was reported by a physician from United States. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: cardiac failure congestive. On
Jan 01, 2008 this consumer started treatment with Digitek 0.125 Mg (dosage: One Daily 047). The following drugs were being taken at the same time: NA. When using Digitek 0.125 Mg, the patient experienced the following unwanted symptoms/side effects: Cardiac Failure Congestive, Condition Aggravated, Therapeutic Agent ToxicityThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Cardiac Failure Congestive, may become evident only after a product is in use by the general population.
Digitek Side Effect Report#5965255-0
Dizziness, Heart Rate Decreased, Hyperhidrosis, Pollakiuria, Product Quality Issue, Pulse Absent, Skin Discolouration, Unresponsive To Stimuli
This Dizziness side effect was reported by a health professional from United States. A 80-year-old male patient (weight:NA) experienced the following symptoms/conditions: atrial fibrillation.The patient was prescribed Digitek 125mcg Bertk (drug dosage: 125mcg Bid Po), which was initiated on
Jan 01, 2006. Concurrently used drugs: NA..After starting to take Digitek 125mcg Bertk the consumer reported adverse symptoms, such as: Dizziness, Heart Rate Decreased, Hyperhidrosis, Pollakiuria, Product Quality Issue, Pulse Absent, Skin Discolouration, Unresponsive To StimuliThese side effects may potentially be related to Digitek 125mcg Bertk. The patient was hospitalized and became disabled.
Digitek Side Effect Report#5964532-7
Abdominal Pain, Mental Disorder, Nausea, Panic Attack, Vomiting
This is a report of a female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: cardiac disorder, who was treated with Digitek (dosage: Rite Aid, start time: NS), combined with:
  • Promethazine
  • Phillips Of Magnesia
  • Ensure High Protein Shakes
and developed a serious reaction and side effect(s): Abdominal Pain, Mental Disorder, Nausea, Panic Attack, Vomiting after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Digitek treatment in female patients, resulting in Abdominal Pain side effect.
Digitek Side Effect Report#5954222-9
Activities Of Daily Living Impaired, Anxiety, Asthenia, Blood Pressure Decreased, Cough, Dyspnoea, Feeling Abnormal, Heart Rate Increased, Hypertension
This report suggests a potential Digitek-bertek Pharm Activities Of Daily Living Impaired side effect(s) that can have serious consequences. A female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: cardiac disorder and used Digitek-bertek Pharm (dosage: 250 Mcg 1 Daily) starting NS. After starting Digitek-bertek Pharm the patient began experiencing various side effects, including: Activities Of Daily Living Impaired, Anxiety, Asthenia, Blood Pressure Decreased, Cough, Dyspnoea, Feeling Abnormal, Heart Rate Increased, HypertensionAdditional drugs used concurrently: NA. Although Digitek-bertek Pharm demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Activities Of Daily Living Impaired, may still occur.
Digitek Side Effect Report#5951428-X
Cardiac Failure Congestive, Fall, Hypotension, Loss Of Consciousness, Oedema Peripheral
This Cardiac Failure Congestive problem was reported by a consumer or non-health professional from United States. A 82-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: atrial fibrillation. On
Nov 01, 2007 this consumer started treatment with Digitek (dosage: 1x A Day). The following drugs were being taken at the same time: NA. When using Digitek, the patient experienced the following unwanted symptoms/side effects: Cardiac Failure Congestive, Fall, Hypotension, Loss Of Consciousness, Oedema PeripheralThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Cardiac Failure Congestive, may become evident only after a product is in use by the general population.
Digitek Side Effect Report#5945978-X
This Death side effect was reported by a health professional from United States. A 59-year-old female patient (weight:NA) experienced the following symptoms/conditions: cardiac disorder.The patient was prescribed Digitek 125 Mcg Actavis Totowa (drug dosage: 125 Mcg One Daily By Mouth), which was initiated on
Jan 11, 2008. Concurrently used drugs: NA..After starting to take Digitek 125 Mcg Actavis Totowa the consumer reported adverse symptoms, such as: These side effects may potentially be related to Digitek 125 Mcg Actavis Totowa.
Digitek Side Effect Report#5939815-7
Heart Rate Decreased, Product Quality Issue
This is a report of a 76-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: NA, who was treated with Digitek 0.25mg Mylan (dosage: 0.25mg Daily Daily Oral, start time: NS), combined with:
  • Torsemide
  • Diltiazem Xr
  • Ciprofloxacin
  • Pantoprazole Sodium
  • Indomethacin
  • Lopressor
  • Cyclosporine
and developed a serious reaction and side effect(s): Heart Rate Decreased, Product Quality Issue after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Digitek 0.25mg Mylan treatment in female patients, resulting in Heart Rate Decreased side effect. The patient was hospitalized.
Digitek Side Effect Report#5924919-5
Diarrhoea, Nausea, Vomiting
This report suggests a potential Digitek .025 Bertek Diarrhoea side effect(s) that can have serious consequences. A 68-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: heart rate increased and used Digitek .025 Bertek (dosage: 1 Daily) starting
Apr 19, 1998. After starting Digitek .025 Bertek the patient began experiencing various side effects, including: Diarrhoea, Nausea, VomitingAdditional drugs used concurrently: NA. Although Digitek .025 Bertek demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Diarrhoea, may still occur.
Digitek Side Effect Report#5924840-2
Incorrect Dose Administered, Product Quality Issue
This Incorrect Dose Administered problem was reported by a consumer or non-health professional from United States. A 96-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: heart rate irregular. On
Oct 04, 2007 this consumer started treatment with Digitek 250 Actovis-in New Jersey Plant (dosage: Daily Po). The following drugs were being taken at the same time: NA. When using Digitek 250 Actovis-in New Jersey Plant, the patient experienced the following unwanted symptoms/side effects: Incorrect Dose Administered, Product Quality IssueThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Incorrect Dose Administered, may become evident only after a product is in use by the general population.
Digitek Side Effect Report#5920940-1
Cardiac Arrest, Product Quality Issue
This Cardiac Arrest side effect was reported by a health professional from United States. A 46-year-old male patient (weight:NA) experienced the following symptoms/conditions: myocardial infarction.The patient was prescribed Digitek 0.125 Mg Tab Bertek Pha (drug dosage: 1 By Mouth Daily), which was initiated on
Nov 19, 2006. Concurrently used drugs: NA..After starting to take Digitek 0.125 Mg Tab Bertek Pha the consumer reported adverse symptoms, such as: Cardiac Arrest, Product Quality IssueThese side effects may potentially be related to Digitek 0.125 Mg Tab Bertek Pha.
Digitek Side Effect Report#5913091-3
Asthenia, Cognitive Disorder, Confusional State, Nausea, Renal Failure, Therapeutic Agent Toxicity, Vomiting
This is a report of a 86-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: cardiac disorder, who was treated with Digitek 0.125mg Bertk (dosage: 1 Tablet Daily Oral, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Asthenia, Cognitive Disorder, Confusional State, Nausea, Renal Failure, Therapeutic Agent Toxicity, Vomiting after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Digitek 0.125mg Bertk treatment in female patients, resulting in Asthenia side effect.
Digitek Side Effect Report#5907624-0
Dizziness Postural, Heart Rate Decreased, Vision Blurred
This report suggests a potential Digitek 125 Mcg Bertek Dizziness Postural side effect(s) that can have serious consequences. A 89-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: atrial fibrillation and used Digitek 125 Mcg Bertek (dosage: 125 Mcg 1 Daily Oral) starting
Mar 29, 2007. After starting Digitek 125 Mcg Bertek the patient began experiencing various side effects, including: Dizziness Postural, Heart Rate Decreased, Vision BlurredAdditional drugs used concurrently: NA.The patient was hospitalized. Although Digitek 125 Mcg Bertek demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dizziness Postural, may still occur.
Digitek Side Effect Report#5892382-9
Asthenia, Blood Pressure Decreased, Dyspnoea, Haemoglobin Decreased, Loss Of Consciousness, Pallor
This Asthenia problem was reported by a consumer or non-health professional from United States. A 88-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: atrial fibrillation. On NS this consumer started treatment with Digitek (dosage: Daily Po). The following drugs were being taken at the same time: NA. When using Digitek, the patient experienced the following unwanted symptoms/side effects: Asthenia, Blood Pressure Decreased, Dyspnoea, Haemoglobin Decreased, Loss Of Consciousness, PallorThe patient was hospitalized and became disabled.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Asthenia, may become evident only after a product is in use by the general population.
Digitek Side Effect Report#5889004-X
Hypotension, Therapeutic Agent Toxicity
This Hypotension side effect was reported by a pharmacist from United States. A 66-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Digitek 0.25mg (drug dosage: 1 Tablet Daily Po), which was initiated on NS. Concurrently used drugs: NA..After starting to take Digitek 0.25mg the consumer reported adverse symptoms, such as: Hypotension, Therapeutic Agent ToxicityThese side effects may potentially be related to Digitek 0.25mg.
Digitek Side Effect Report#5887379-9
Agitation, Anorexia, Confusional State, Disturbance In Attention, Dyspnoea, Fluid Retention, Hypersomnia, Hypotension, Lethargy
This is a report of a 64-year-old male patient (weight: NA) from United States, suffering from the following health symptoms/conditions: cardiac failure congestive, who was treated with Digitek .25 Mg Bertek (actual Dose Was .50 Mg (dosage: .25 Each Night Many Years, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Agitation, Anorexia, Confusional State, Disturbance In Attention, Dyspnoea, Fluid Retention, Hypersomnia, Hypotension, Lethargy after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Digitek .25 Mg Bertek (actual Dose Was .50 Mg treatment in male patients, resulting in Agitation side effect. The patient was hospitalized.


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The appearance of Digitek on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

What are common Digitek Side Effects for Women?

Women Side EffectsReports
Dizziness 113
Nausea 92
Asthenia 66
Vomiting 46
Fatigue 38
Heart Rate Decreased 37
Hypotension 37
Fall 35
Diarrhoea 34
Therapeutic Agent Toxicity 34

What are common Digitek Side Effects for Men?

Men Side EffectsReports
Dizziness 96
Nausea 63
Fatigue 47
Hypotension 39
Asthenia 36
Dyspnoea 35
Diarrhoea 28
Vomiting 25
Heart Rate Decreased 23
Therapeutic Agent Toxicity 22

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Digitek reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

    Discuss Digitek Side Effects

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    How Effective is Digitek for You?

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    Digitek Safety Alerts, Active Ingredients, Usage Information

    NDC0378-6155
    TypeHUMAN PRESCRIPTION DRUG
    Proprietary NameDIGITEK
    Namedigoxin
    Dosage FormTABLET
    RouteORAL
    On market since20141117
    LabelerMylan Pharmaceuticals Inc.
    Active Ingredient(s)DIGOXIN
    Strength(s)0.125
    Unit(s)mg/1
    Pharma ClassCardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]

    More About Digitek

    Side Effects reported to FDA: 606

    Digitek safety alerts: 2008

    Reported deaths: 27

    Reported hospitalizations: 31

    Digitek (digoxin tablets, USP)

    Audience: Cardiologists, family physicians, pharmacists, other healthcare professionals, patients

    [Posted 04/28/2008] Actavis Totowa LLC notified healthcare professionals of a Class I nationwide recall of all strengths of Digitek, a drug used to treat heart failure and abnormal heart rhythms. The products are distributed by Mylan Pharmaceuticals Inc., under a ‚??Bertek‚?Ě label and by UDL Laboratories, Inc. under a ‚??UDL‚?Ě label. The product is being recalled due to the possibility that tablets with double the appropriate thickness may contain twice the approved level of active ingredient. The existence of double strength tablets poses a risk of digitalis toxicity in patents with renal failure. Digitalis toxicity can cause nausea, vomiting, dizziness, low blood pressure, cardiac instability and bradycardia. Several reports of illnesses and injuries have been reported. Patients should contact their healthcare professional with questions.

    [April 25, 2008 - Press Release - Actavis Totowa LLC]

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