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Orbenine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 9. View All

Orbenine FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 9

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

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6135542-4 | Agranulocytosis, Bone Marrow Failure, Breast Abscess, Coagulopathy, Hyperbilirubinaemia, Renal Failure Acute, Septic Rash, Ulcer
on Mar 18, 2009 Female patient from SPAIN , 59 years of age, was diagnosed with superinfection, herpes zoster, prophylaxis and was treated with Orbenine (View Usage). Patient experienced the following unwanted or unexpected effects: agranulocytosis, bone marrow failure, breast abscess, coagulopathy, hyperbilirubinaemia, renal failure acute, septic rash, ulcer (What is ulcer?). Orbenine dosage: . During the same period patient was treated with AMOXICILLIN AND CLAVULANATE POTASSIUM (View Amoxicillin And Clavulanate Potassium Review and Amoxicillin And Clavulanate Potassium Label ), BRIVUDINE (View Brivudine Review and Brivudine Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6077329-7 | Blister, Diarrhoea, Lung Disorder, Oedema, Purpura, Pyrexia, Rash, Skin Disorder
Patient was taking Orbenine (View Usage). Patient had the following side effects: blister, diarrhoea, lung disorder, oedema, purpura, pyrexia, rash (What is rash?), skin disorder on Feb 12, 2009 from FRANCE Additional patient health information: Female patient , 21 years of age, was diagnosed with erythrosis and. Orbenine dosage: 1g Twice Per Day. During the same period patient was treated with PYOSTACINE (1g Twice Per Day) (View Pyostacine Review and Pyostacine Label ), XYZAL (10mg Per Day) (View Xyzal Review and Xyzal Label ), FUCIDINE CAP (View Fucidine Cap Review and Fucidine Cap Label ), DIASEPTYL (View Diaseptyl Review and Diaseptyl Label ), EFFICORT (View Efficort Review and Efficort Label ), MUPIDERM (View Mupiderm Review and Mupiderm Label ), PIPERACILLINE (View Piperacilline Review and Piperacilline Label ), TAZOCILLINE (View Tazocilline Review and Tazocilline Label ). Patient was hospitalized.

6066625-5 | Blister, Diarrhoea, Oedema, Purpura, Pyrexia, Skin Disorder, Skin Exfoliation, Skin Lesion
Adverse event was reported on Jan 30, 2009 by a Female patient taking Orbenine (View Usage) (Dosage: 1g Twice Per Day) was diagnosed with erythrosis and. Location: FRANCE , 21 years of age, After Orbenine was administered, patient had the following side effects: blister, diarrhoea, oedema, purpura, pyrexia, skin disorder, skin exfoliation, skin lesion. During the same period patient was treated with PYOSTACINE (1g Twice Per Day) (View Pyostacine Review and Pyostacine Label ), XYZAL (10mg Per Day) (View Xyzal Review and Xyzal Label ), FUCIDINE CAP (View Fucidine Cap Review and Fucidine Cap Label ), DIASEPTYL (View Diaseptyl Review and Diaseptyl Label ), EFFICORT (View Efficort Review and Efficort Label ), MUPIDERM (View Mupiderm Review and Mupiderm Label ), AUREOMYCINE (View Aureomycine Review and Aureomycine Label ), CELESTAMINE TAB (View Celestamine Tab Review and Celestamine Tab Label ). Patient was hospitalized.

5761163-9 | Anuria, Dermatitis, Renal Failure Acute, Venous Stasis
on Jun 05, 2008 Female patient from FRANCE , 82 years of age, was diagnosed with erysipelas and was treated with Orbenine (View Usage). Patient experienced the following unwanted or unexpected effects: anuria, dermatitis, renal failure acute, venous stasis. Orbenine dosage: 3g Per Day. During the same period patient was treated with AMOXICILLIN AND CLAVULANATE POTASSIUM (View Amoxicillin And Clavulanate Potassium Review and Amoxicillin And Clavulanate Potassium Label ), PREVISCAN (1tab Per Day) (View Previscan Review and Previscan Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), COZAAR (1tab Per Day) (View Cozaar Review and Cozaar Label ), MOPRAL (1tab Per Day) (View Mopral Review and Mopral Label ), LASILIX (1g Per Day) (View Lasilix Review and Lasilix Label ), ALDOMET (1tab Per Day) (View Aldomet Review and Aldomet Label ), NITRODERM (1pat Per Day) (View Nitroderm Review and Nitroderm Label ). Patient was hospitalized.


5750859-0 | Angioedema, Blood Pressure Decreased, Cough, Pharyngeal Oedema, Urticaria
on May 23, 2008 Female patient from FRANCE , 71 years of age, was diagnosed with bronchopneumopathy and was treated with Orbenine (View Usage). Patient had the following side effects: angioedema, blood pressure decreased, cough, pharyngeal oedema, urticaria. Orbenine dosage: 1g Per Day. During the same period patient was treated with AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), SERETIDE (View Seretide Review and Seretide Label ), VENTOLIN (View Ventolin Review and Ventolin Label ). Patient was hospitalized.

5723580-2 | Anuria, Dermatitis, Renal Failure Acute, Venous Stasis
Patient was taking Orbenine (View Usage). After Orbenine was administered, patient had the following side effects: anuria, dermatitis, renal failure acute, venous stasis on Apr 28, 2008 from FRANCE Additional patient health information: Female patient , 82 years of age, was diagnosed with erysipelas and. Orbenine dosage: 3g Per Day. During the same period patient was treated with AMOXICILLIN AND CLAVULANATE POTASSIUM (View Amoxicillin And Clavulanate Potassium Review and Amoxicillin And Clavulanate Potassium Label ), PREVISCAN (1tab Per Day) (View Previscan Review and Previscan Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), COZAAR (1tab Per Day) (View Cozaar Review and Cozaar Label ), OMEPRAZOLE (1tab Per Day) (View Omeprazole Review and Omeprazole Label ), LASILIX (1g Per Day) (View Lasilix Review and Lasilix Label ), ALDOMET (1tab Per Day) (View Aldomet Review and Aldomet Label ), NITRODERM (1pat Per Day) (View Nitroderm Review and Nitroderm Label ). Patient was hospitalized.

5001845-X | Asthenia, Cardiac Arrest, Hypotension, Melaena, Pancytopenia, Polyuria
Adverse event was reported on Apr 10, 2006 by a Male patient taking Orbenine (View Usage) (Dosage: ) . Location: FRANCE , 67 years of age, weighting 264.6 lb, Patient experienced the following unwanted or unexpected effects: asthenia, cardiac arrest (What is cardiac arrest?), hypotension, melaena, pancytopenia, polyuria. During the same period patient was treated with AUGMENTIN '125' (1g Three Times Per Day) (View Augmentin '125' Review and Augmentin '125' Label ), OFLOCET (View Oflocet Review and Oflocet Label ), GENTALLINE (120mg Twice Per Day) (View Gentalline Review and Gentalline Label ), COLCHIMAX (View Colchimax Review and Colchimax Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), TAHOR (View Tahor Review and Tahor Label ), RENITEC (View Renitec Review and Renitec Label ), DIGOXIN (View Digoxin Review and Digoxin Label ). Patient was hospitalized.

4981816-X | Asthenia, Cardiac Arrest, Hypotension, Melaena, Pancytopenia, Polyuria
on Apr 10, 2006 Male patient from FRANCE , 67 years of age, weighting 264.6 lb, was treated with Orbenine (View Usage). Patient had the following side effects: asthenia, cardiac arrest (What is cardiac arrest?), hypotension, melaena, pancytopenia, polyuria. Orbenine dosage: . During the same period patient was treated with AUGMENTIN '125' (1g Three Times Per Day) (View Augmentin '125' Review and Augmentin '125' Label ), OFLOCET (View Oflocet Review and Oflocet Label ), GENTALLINE (120mg Twice Per Day) (View Gentalline Review and Gentalline Label ), COLCHIMAX (View Colchimax Review and Colchimax Label ), ZYLORIC (View Zyloric Review and Zyloric Label ), TAHOR (View Tahor Review and Tahor Label ), RENITEC (View Renitec Review and Renitec Label ), DIGOXIN (View Digoxin Review and Digoxin Label ). Patient was hospitalized.

4865193-0 | Alanine Aminotransferase Increased, Cytolytic Hepatitis, Eosinophilia, Prothrombin Time Prolonged, Purpura, Pyrexia, Toxic Skin Eruption
on Mar 09, 2004 Male patient from FRANCE , 28 years of age, was diagnosed with pharyngitis, leishmaniasis (What is leishmaniasis?) and was treated with Orbenine (View Usage). After Orbenine was administered, patient had the following side effects: alanine aminotransferase increased, cytolytic hepatitis, eosinophilia, prothrombin time prolonged, purpura, pyrexia, toxic skin eruption. Orbenine dosage: 500mg Per Day. During the same period patient was treated with ZINNAT (500mg Per Day) (View Zinnat Review and Zinnat Label ), PENTACARINAT (300mg Per Day) (View Pentacarinat Review and Pentacarinat 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 Orbenine 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 Orbenine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Orbenine 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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Orbenine Reactions
Agranulocytosis
Alanine Aminotransferase Increased
Angioedema
Anuria
Asthenia
Blister
Blood Pressure Decreased
Bone Marrow Failure
Breast Abscess
Cardiac ArrestWhat is Cardiac arrest?
Coagulopathy
Cough
Cytolytic Hepatitis
Dermatitis
Diarrhoea
Eosinophilia
Hyperbilirubinaemia
Hypotension
Lung Disorder
Melaena
Oedema
Pancytopenia
Pharyngeal Oedema
Polyuria
Prothrombin Time Prolonged
Purpura
Pyrexia
Renal Failure Acute
Skin Disorder
Venous Stasis
Orbenine 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 Orbenine 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!