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Teralithe adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Teralithe FDA safety alerts: No

Reported hospitalizations: 2

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

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5241447-3 | Agitation, Arrhythmia Supraventricular, Atrioventricular Block, Azotaemia, Blood Creatinine Increased, Bradycardia, Dehydration, Electrocardiogram Pr Prolongation
on Feb 06, 2007 Male patient from , 42 years of age, was diagnosed with agitation, thrombosis prophylaxis and was treated with Teralithe (View Usage). Patient experienced the following unwanted or unexpected effects: agitation, arrhythmia supraventricular, atrioventricular block, azotaemia, blood creatinine increased, bradycardia, dehydration, electrocardiogram pr prolongation. Teralithe dosage: . During the same period patient was treated with TERCIAN /00759301/ (View Tercian /00759301/ Review and Tercian /00759301/ Label ), LOVENOX (View Lovenox Review and Lovenox Label ), TRANXENE (View Tranxene Review and Tranxene Label ). Patient was hospitalized.

4644752-4 | Agitation, Asthenia, Blood Creatinine Decreased, Confusional State, Depressed Level Of Consciousness, Disorientation, Extrapyramidal Disorder, Fall
Patient was taking Teralithe (View Usage). Patient had the following side effects: agitation, asthenia, blood creatinine decreased, confusional state, depressed level of consciousness, disorientation, extrapyramidal disorder, fall (What is fall?) on Apr 14, 2005 from Additional patient health information: Female patient , 73 years of age, was diagnosed with bipolar i disorder, diabetes mellitus, hypothyroidism and. Teralithe dosage: . During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), FLUOROURACIL (View Fluorouracil Review and Fluorouracil Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ), MOPRAL (View Mopral Review and Mopral Label ), DIFFU K (View Diffu K Review and Diffu K Label ), FORLAX (View Forlax Review and Forlax Label ), SPASFON (View Spasfon Review and Spasfon Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ). 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 Teralithe 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 Teralithe quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Teralithe 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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... The First Trimester Of Pregnancy) (View Atarax Review and Atarax Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), TERALITHE ...<<<<

During the same period patient was treated with TERALITHE (View Teralithe Review and Teralithe Label ). 6360736-2 | Condition Aggravated, Epilepsy<<<<

During the same period patient was treated with TERALITHE (View Teralithe Review and Teralithe Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), LEVOTHYROX ...<<<<

During the same period patient was treated with TERALITHE. Patient was hospitalized. Fosfomycin Side Effects Report: 6335609-1,Dermatitis Allergic, Hypersensitivity ...<<<<

During the same period patient was treated with EFFEXOR (Dose Reduced By 2 On Mid Dec2009) (View Effexor Review and Effexor Label ), TERALITHE (View Teralithe Review and ...<<<<

During the same period patient was treated with TERALITHE (Total Daily Dose: 300 Mg Unit Dose: 300 Mg) (View Teralithe Review and Teralithe Label ), CRESTOR (Total Daily ...<<<<

During the same period patient was treated with TERALITHE (View Teralithe Review and Teralithe Label ). Patient was hospitalized. 5211925-1 | Cryptogenic Organising ...<<<<

)During the same period patient was treated with TERALITHE (750mg Daily) (View Teralithe Review and Teralithe Label ), TERCIAN (25 Mg, 1x/day) (View Tercian Review and Tercian ...<<<<

During the same period patient was treated with TERALITHE (View Teralithe Review and Teralithe Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), LEVOTHYROX ...<<<<

During the same period patient was treated with TERALITHE (View Teralithe Review and Teralithe Label ), EFFEXOR (View Effexor Review and Effexor Label ).<<<<

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Teralithe Reactions
Agitation
Arrhythmia Supraventricular
Asthenia
Atrioventricular Block
Azotaemia
Blood Creatinine Decreased
Blood Creatinine Increased
Bradycardia
Confusional State
Dehydration
Depressed Level Of Consciousness
Disorientation
Electrocardiogram Pr Prolongation
Extrapyramidal Disorder
FallWhat is Fall?
Teralithe 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 Teralithe 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!