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Summary

FDA Adverse Reports: 1. View All

Tenectaplase FDA safety alerts: No

Reported hospitalizations: 1

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

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5308113-7 | Aneurysm, Haemorrhage Intracranial, Neurological Symptom, Respiratory Failure
on Apr 23, 2007 Male patient from UNITED STATES , 63 years of age, weighting 220.5 lb, was diagnosed with myocardial infarction and was treated with Tenectaplase (View Usage). Patient experienced the following unwanted or unexpected effects: aneurysm (What is aneurysm?), haemorrhage intracranial, neurological symptom, respiratory failure. Tenectaplase dosage: Given At Another Hospital. 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 Tenectaplase 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 Tenectaplase quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tenectaplase 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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Eighty percent of patients received a fibrin-specific agent (19% tenecteplase, 5% reteplase and 55% alteplase) and 20% received streptokinase.<<<<

During the same period patient was treated with TENECTEPLASE 50MG (50mg One Time Iv Bolus) (View Tenecteplase 50mg Review and Tenecteplase 50mg Label ).<<<<

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Tenectaplase Reactions
AneurysmWhat is Aneurysm?
Haemorrhage Intracranial
Neurological Symptom
Respiratory Failure
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