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Protenate adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Protenate FDA safety alerts: No

Reported hospitalizations: 2

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

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5795246-4 | Hepatitis B
on Jun 13, 2008 Female patient from JAPAN , 26 years of age, weighting 105.8 lb, was diagnosed with shock haemorrhagic and was treated with Protenate (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis b (What is hepatitis b?). Protenate dosage: . During the same period patient was treated with FRESH FROZEN PLASMA (View Fresh Frozen Plasma Review and Fresh Frozen Plasma Label ), RED BLOOD CELLS (View Red Blood Cells Review and Red Blood Cells Label ).

5778931-X | Hepatitis B
Patient was taking Protenate (View Usage). Patient had the following side effects: hepatitis b (What is hepatitis b?) on Jun 11, 2008 from JAPAN Additional patient health information: Female patient , 69 years of age, was diagnosed with hypoalbuminaemia, haemorrhage and. Protenate dosage: . During the same period patient was treated with MAPROTILINE HYDROCHLORIDE (View Maprotiline Hydrochloride Review and Maprotiline Hydrochloride Label ), FRESH FROZEN PLASMA (View Fresh Frozen Plasma Review and Fresh Frozen Plasma Label ).

5774467-0 | Hepatitis B
Adverse event was reported on Jun 06, 2008 by a Female patient taking Protenate (View Usage) (Dosage: ) was diagnosed with hypoalbuminaemia, haemorrhage and. Location: JAPAN , 69 years of age, After Protenate was administered, patient had the following side effects: hepatitis b (What is hepatitis b?). During the same period patient was treated with MAPROTILINE HYDROCHLORIDE (View Maprotiline Hydrochloride Review and Maprotiline Hydrochloride Label ), FRESH FROZEN PLASMA (View Fresh Frozen Plasma Review and Fresh Frozen Plasma Label ).

5197059-3 | Anaphylactic Shock, Dialysis Device Complication, Thrombosis
on Nov 29, 2006 Male patient from JAPAN , 66 years of age, weighting 151.0 lb, was diagnosed with prophylaxis and was treated with Protenate (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, dialysis device complication, thrombosis. Protenate dosage: 250 Ml; Unk; Iv. During the same period patient was treated with SALINE (View Saline Review and Saline Label ). Patient was hospitalized.


5110805-X | Anaphylactic Shock, Ill-defined Disorder, Procedural Complication, Thrombosis In Device
on Aug 31, 2006 Male patient from JAPAN , 66 years of age, weighting 151.0 lb, was diagnosed with prophylaxis and was treated with Protenate (View Usage). Patient had the following side effects: anaphylactic shock, ill-defined disorder, procedural complication, thrombosis in device. Protenate dosage: 250 Ml; Iv. During the same period patient was treated with SALINE (View Saline Review and Saline 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 Protenate 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 Protenate quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Protenate 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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protenate Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: protonix Episodes: 2: Diagnosed with major depression.Side ...

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Protenate Reactions
Anaphylactic Shock
Dialysis Device Complication
Hepatitis BWhat is Hepatitis b?
Ill-defined Disorder
Procedural Complication
Thrombosis
Thrombosis In Device
Protenate 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 Protenate 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!