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Tyzeka adverse events reported to FDA.

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Summary

FDA Adverse Reports: 16. View All

Tyzeka FDA safety alerts: No

Reported hospitalizations: 3

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

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6614090-9 | Blood Creatine Phosphokinase Increased, Gingival Bleeding, Lipids Increased, Myalgia, Rhabdomyolysis
on Feb 23, 2010 Male patient from UNITED STATES , 55 years of age, was diagnosed with hepatitis b (What is hepatitis b?), lipids increased and was treated with Tyzeka (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, gingival bleeding, lipids increased, myalgia, rhabdomyolysis. Tyzeka dosage: 600 Mg, Qw4. During the same period patient was treated with LIPITOR (5 Mg, Qd) (View Lipitor Review and Lipitor Label ), LOPID (600 Mg, Bid) (View Lopid Review and Lopid Label ), METOPROLOL TARTRATE (1000 Mg, Unk) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ). Patient was hospitalized.

5988679-4 | Cardiomyopathy, Echocardiogram Abnormal, Left Ventricular Dysfunction
Patient was taking Tyzeka (View Usage). Patient had the following side effects: cardiomyopathy (What is cardiomyopathy?), echocardiogram abnormal, left ventricular dysfunction on Dec 01, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 171.0 lb, was diagnosed with hepatitis b (What is hepatitis b?) and. Tyzeka dosage: 600 Mg, After Every Other Dialysis.

5816060-7 | Burning Sensation, Hypoaesthesia, Muscle Spasms, Neuropathy Peripheral, Pain, Paraesthesia, Vibration Test Abnormal
Adverse event was reported on Jul 11, 2008 by a Female patient taking Tyzeka (View Usage) (Dosage: 600 Mg, Qd) was diagnosed with hepatitis b virus test and. Location: UNITED KINGDOM , weighting 97.89 lb, After Tyzeka was administered, patient had the following side effects: burning sensation, hypoaesthesia, muscle spasms, neuropathy peripheral, pain (What is pain?), paraesthesia, vibration test abnormal. During the same period patient was treated with COMPARATOR PEGASYS (180 Mcg Weekly) (View Comparator Pegasys Review and Comparator Pegasys Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), CHLORAMPHENICOL (View Chloramphenicol Review and Chloramphenicol Label ), SENNA (Unk) (View Senna Review and Senna Label ), FYBOGEL (View Fybogel Review and Fybogel Label ), BISACODYL (View Bisacodyl Review and Bisacodyl Label ), FERROUS SULFATE TAB (View Ferrous Sulfate Tab Review and Ferrous Sulfate Tab Label ).

5809492-4 | Carpal Tunnel Syndrome, Hypoaesthesia, Myalgia, Peripheral Sensory Neuropathy, Radiculopathy
on Jul 04, 2008 Male patient from TAIWAN, PROVINCE OF CHINA , weighting 160.9 lb, was diagnosed with hepatitis b (What is hepatitis b?) and was treated with Tyzeka (View Usage). Patient experienced the following unwanted or unexpected effects: carpal tunnel syndrome (What is carpal tunnel syndrome?), hypoaesthesia, myalgia, peripheral sensory neuropathy, radiculopathy. Tyzeka dosage: 600 Mg,. During the same period patient was treated with COMPARATOR PEGASYS (180 Ug,) (View Comparator Pegasys Review and Comparator Pegasys Label ).


5802675-9 | Hypoaesthesia, Radiculopathy
on Jul 04, 2008 Male patient from SINGAPORE , weighting 118.4 lb, was diagnosed with hepatitis b (What is hepatitis b?) and was treated with Tyzeka (View Usage). Patient had the following side effects: hypoaesthesia, radiculopathy. Tyzeka dosage: 600 Mg, Unk.

5801609-0 | Polyneuropathy
Patient was taking Tyzeka (View Usage). After Tyzeka was administered, patient had the following side effects: polyneuropathy on Jun 25, 2008 from ISRAEL Additional patient health information: Female patient , weighting 163.1 lb, was diagnosed with hepatitis b (What is hepatitis b?) and. Tyzeka dosage: 600 Mg,.

5795850-3 | Angiopathy, Hypoaesthesia
Adverse event was reported on Jun 19, 2008 by a Male patient taking Tyzeka (View Usage) (Dosage: 600 Mg, Unk) was diagnosed with hepatitis b (What is hepatitis b?) and. Location: SINGAPORE , weighting 118.4 lb, Patient experienced the following unwanted or unexpected effects: angiopathy, hypoaesthesia.

5792726-2 | Electromyogram Abnormal, Neuropathy Peripheral
on Mar 05, 2008 Male patient from UNITED STATES , 38 years of age, weighting 170.0 lb, was diagnosed with hepatitis b (What is hepatitis b?) and was treated with Tyzeka (View Usage). Patient had the following side effects: electromyogram abnormal, neuropathy peripheral. Tyzeka dosage: 600 Mg, Qd, Oral. During the same period patient was treated with PEGASYS (View Pegasys Review and Pegasys Label ), CELEXA (View Celexa Review and Celexa Label ).

5765743-6 | Asthenia, Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Hyperreflexia, Muscle Atrophy, Polymyositis, Weight Decreased
on Jun 06, 2008 Male patient from SINGAPORE , weighting 119.0 lb, was diagnosed with hepatitis b (What is hepatitis b?), hypertension and was treated with Tyzeka (View Usage). After Tyzeka was administered, patient had the following side effects: asthenia, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, hyperreflexia, muscle atrophy, polymyositis, weight decreased. Tyzeka dosage: 600 Mg,. During the same period patient was treated with METOPROLOL (View Metoprolol Review and Metoprolol Label ). Patient was hospitalized.

5765721-7 | Asthenia, Pain, Paraesthesia, Peripheral Sensory Neuropathy, Sensory Loss
Patient was taking Tyzeka (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, pain (What is pain?), paraesthesia, peripheral sensory neuropathy, sensory loss on Jun 02, 2008 from ISRAEL Additional patient health information: Male patient , weighting 119.0 lb, was diagnosed with hepatitis b (What is hepatitis b?) and. Tyzeka dosage: 600 Mg,. During the same period patient was treated with PEGASYS (180 Mcg) (View Pegasys Review and Pegasys Label ). Patient was hospitalized.

5764778-7 | Caesarean Section, Normal Newborn
Adverse event was reported on Jun 03, 2008 by a Female patient taking Tyzeka (View Usage) (Dosage: 600 Mg, Unk) was diagnosed with hepatitis b (What is hepatitis b?) and. Location: UNITED STATES , weighting 149.0 lb, Patient had the following side effects: caesarean section, normal newborn. During the same period patient was treated with TRUVADA (500 Mg, Unk) (View Truvada Review and Truvada Label ), VITAMINS (View Vitamins Review and Vitamins Label ).

5762319-1 | Blood Creatine Phosphokinase Increased, Myalgia, Myositis, Paraesthesia, Peripheral Sensory Neuropathy
on May 29, 2008 Male patient from ARGENTINA , weighting 206.1 lb, was diagnosed with hepatitis b (What is hepatitis b?) and was treated with Tyzeka (View Usage). After Tyzeka was administered, patient had the following side effects: blood creatine phosphokinase increased, myalgia, myositis (What is myositis?), paraesthesia, peripheral sensory neuropathy. Tyzeka dosage: 600 Mg, Qd. During the same period patient was treated with PEGASYS (180 Ug, Qw) (View Pegasys Review and Pegasys Label ).

5730214-X | Neuropathy Peripheral
on Feb 23, 2008 Male patient from UNITED STATES , 38 years of age, was diagnosed with hepatitis b (What is hepatitis b?) and was treated with Tyzeka (View Usage). Patient experienced the following unwanted or unexpected effects: neuropathy peripheral. Tyzeka dosage: Oral. During the same period patient was treated with PEGASYS (View Pegasys Review and Pegasys Label ).

5730183-2 | Electromyogram Abnormal, Neuropathy Peripheral
Patient was taking Tyzeka (View Usage). Patient had the following side effects: electromyogram abnormal, neuropathy peripheral on Mar 24, 2008 from UNITED STATES Additional patient health information: Male patient , 38 years of age, weighting 170.0 lb, was diagnosed with hepatitis b (What is hepatitis b?) and. Tyzeka dosage: 600 Mg, Qd, Oral. During the same period patient was treated with PEGASYS (View Pegasys Review and Pegasys Label ), CELEXA (View Celexa Review and Celexa Label ).

5507843-1 | Delivery, Dyspnoea, Fatigue, Somnolence
Adverse event was reported on Aug 14, 2007 by a Female patient taking Tyzeka (View Usage) (Dosage: 600 Mg, Qd, Oral) was diagnosed with hepatitis b (What is hepatitis b?) and. Location: UNITED STATES , 30 years of age, After Tyzeka was administered, patient had the following side effects: delivery, dyspnoea, fatigue, somnolence.

5507841-8 | Rash Maculo-papular
on Aug 27, 2007 Male patient from UNITED STATES , 48 years of age, was diagnosed with hepatitis b (What is hepatitis b?) and was treated with Tyzeka (View Usage). Patient experienced the following unwanted or unexpected effects: rash maculo-papular. Tyzeka dosage: 600 Mg; Qd; Oral.


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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 Tyzeka 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 Tyzeka quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tyzeka 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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Tyzeka Reactions
Angiopathy
Asthenia
Blood Creatine Phosphokinase Increased
Blood Lactate Dehydrogenase Increased
Burning Sensation
Caesarean Section
CardiomyopathyWhat is Cardiomyopathy?
Carpal Tunnel SyndromeWhat is Carpal tunnel syndrome?
Delivery
Dyspnoea
Echocardiogram Abnormal
Electromyogram Abnormal
Fatigue
Gingival Bleeding
Hyperreflexia
Hypoaesthesia
Left Ventricular Dysfunction
Lipids Increased
Muscle Atrophy
Muscle Spasms
Myalgia
MyositisWhat is Myositis?
Neuropathy Peripheral
Normal Newborn
PainWhat is Pain?
Paraesthesia
Peripheral Sensory Neuropathy
Polymyositis
Polyneuropathy
Radiculopathy
Tyzeka 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 Tyzeka 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!