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Benefix adverse events reported to FDA.

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Summary

FDA Adverse Reports: 182. View All

Benefix FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 62

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

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7006562-2 | Erythema, Rash Pruritic, Urticaria
on Apr 03, 2009 Male patient from UNITED STATES , 53 years of age, weighting 233.7 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, rash pruritic, urticaria. Benefix dosage: . During the same period patient was treated with TRUVADA (View Truvada Review and Truvada Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LYRICA (View Lyrica Review and Lyrica Label ), VIRAMUNE (View Viramune Review and Viramune Label ), AVINZA (View Avinza Review and Avinza Label ).

7006561-0 | Infusion Site Urticaria
Patient was taking Benefix (View Usage). Patient had the following side effects: infusion site urticaria on Mar 27, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 81.57 lb, was diagnosed with factor ix deficiency and. Benefix dosage: .

7006555-5 | Injection Site Pain, Injection Site Rash
Adverse event was reported on Oct 01, 2008 by a Male patient taking Benefix (View Usage) (Dosage: Not Provided) was diagnosed with factor ix deficiency and. Location: UNITED STATES , child 11 years of age, After Benefix was administered, patient had the following side effects: injection site pain, injection site rash.

7006550-6 | Injection Site Pain
on May 27, 2008 Male patient from UNITED STATES , weighting 147.1 lb, was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: injection site pain. Benefix dosage: ~4500 - 5000 Units-the Patient Specifically Requests 9 X 500 Unit Vials. During the same period patient was treated with BENADRYL (View Benadryl Review and Benadryl Label ), TYLENOL (View Tylenol Review and Tylenol Label ).


7006549-X | Cough, Irritability, Respiration Abnormal
on Jul 13, 2009 Male patient from UNITED STATES , weighting 30.03 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient had the following side effects: cough, irritability, respiration abnormal. Benefix dosage: .

7006548-8 | Injection Site Erythema, Injection Site Pain
Patient was taking Benefix (View Usage). After Benefix was administered, patient had the following side effects: injection site erythema, injection site pain on Feb 28, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 33.07 lb, was diagnosed with haemophilia and. Benefix dosage: .

7004941-0 | Infusion Related Reaction, Lethargy, Nausea, Urticaria
Adverse event was reported on Sep 20, 2010 by a Male patient taking Benefix (View Usage) (Dosage: Once Iv) was diagnosed with factor ix deficiency and. Location: UNITED STATES , weighting 30.86 lb, Patient experienced the following unwanted or unexpected effects: infusion related reaction, lethargy, nausea (What is nausea?), urticaria. Patient was hospitalized.

6963776-5 | Cellulitis, Extravasation, Thrombophlebitis Superficial
on Aug 23, 2010 Male patient from UNITED STATES , 49 years of age, was diagnosed with factor ix deficiency, joint swelling and was treated with Benefix (View Usage). Patient had the following side effects: cellulitis (What is cellulitis?), extravasation, thrombophlebitis superficial. Benefix dosage: 2500 Units. Patient was hospitalized.

6900638-3 | Abnormal Sensation In Eye, Anaphylactic Reaction, Ocular Hyperaemia, Sensory Disturbance, Tachycardia, Tension
on Jul 23, 2010 Male patient from BELGIUM , 32 years of age, weighting 154.3 lb, was diagnosed with haemophilia b with anti factor ix and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: abnormal sensation in eye, anaphylactic reaction, ocular hyperaemia, sensory disturbance, tachycardia, tension. Benefix dosage: Not Provided.

6878505-3 | Convulsion, Streptococcal Sepsis
Patient was taking Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, streptococcal sepsis on Jul 22, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 107.8 lb, was diagnosed with factor ix deficiency and. Benefix dosage: 5980 Unit Every 1 Day. Patient was hospitalized.

6827120-6 | Alpha Haemolytic Streptococcal Infection, Bacteraemia, Convulsion, Pyrexia
Adverse event was reported on Jul 02, 2010 by a Male patient taking Benefix (View Usage) (Dosage: ) was diagnosed with factor ix deficiency and. Location: UNITED STATES , weighting 107.8 lb, Patient had the following side effects: alpha haemolytic streptococcal infection, bacteraemia, convulsion, pyrexia. Patient was hospitalized.

6817881-4 | Blood Pressure Decreased, Cold Sweat, Heart Rate Decreased, Nausea, Pallor, Vertigo
on Jun 25, 2010 Male patient from GERMANY , weighting 191.8 lb, was diagnosed with tooth extraction, factor ix deficiency and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: blood pressure decreased, cold sweat, heart rate decreased, nausea (What is nausea?), pallor, vertigo. Benefix dosage: .

6773026-0 | Abnormal Sensation In Eye, Anaphylactic Reaction, Ocular Hyperaemia, Sensory Disturbance, Tachycardia, Tension
on Jun 03, 2010 Male patient from BELGIUM , 32 years of age, weighting 154.3 lb, was diagnosed with haemophilia b with anti factor ix and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal sensation in eye, anaphylactic reaction, ocular hyperaemia, sensory disturbance, tachycardia, tension. Benefix dosage: Not Provided.

6765401-5 | Abnormal Sensation In Eye, Anaphylactic Reaction, Ocular Hyperaemia, Sensory Disturbance, Tachycardia, Tension
Patient was taking Benefix (View Usage). Patient had the following side effects: abnormal sensation in eye, anaphylactic reaction, ocular hyperaemia, sensory disturbance, tachycardia, tension on Jun 03, 2010 from BELGIUM Additional patient health information: Male patient , 32 years of age, weighting 154.3 lb, was diagnosed with haemophilia b with anti factor ix and. Benefix dosage: Not Provided.

6755462-1 | Alpha Haemolytic Streptococcal Infection, Bacteraemia, Convulsion, Pyrexia
Adverse event was reported on Jun 01, 2010 by a Male patient taking Benefix (View Usage) (Dosage: ) was diagnosed with factor ix deficiency and. Location: UNITED STATES , weighting 107.8 lb, After Benefix was administered, patient had the following side effects: alpha haemolytic streptococcal infection, bacteraemia, convulsion, pyrexia. Patient was hospitalized.

6750815-X | Bacteraemia, Convulsion, Pyrexia
on May 25, 2010 Male patient from UNITED STATES , weighting 107.8 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: bacteraemia, convulsion, pyrexia. Benefix dosage: . Patient was hospitalized.

6743277-X | Factor Ix Inhibition
on May 17, 2010 Male patient from UNITED STATES , weighting 24.69 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient had the following side effects: factor ix inhibition. Benefix dosage: 1000 Units Ivp As Needed.

6733597-7 | Bacteraemia, Convulsion, Pyrexia, Streptococcal Infection
Patient was taking Benefix (View Usage). After Benefix was administered, patient had the following side effects: bacteraemia, convulsion, pyrexia, streptococcal infection (What is streptococcal infection?) on May 11, 2010 from UNITED STATES Additional patient health information: Male patient , child 11 years of age, was diagnosed with factor ix deficiency and. Benefix dosage: . Patient was hospitalized.

6733594-1 | Abnormal Sensation In Eye, Anaphylactic Reaction, Ocular Hyperaemia, Sensory Disturbance, Tachycardia, Tension
Adverse event was reported on May 11, 2010 by a Male patient taking Benefix (View Usage) (Dosage: Not Provided) was diagnosed with haemophilia b with anti factor ix and. Location: BELGIUM , 32 years of age, weighting 154.3 lb, Patient experienced the following unwanted or unexpected effects: abnormal sensation in eye, anaphylactic reaction, ocular hyperaemia, sensory disturbance, tachycardia, tension.

6721066-X | Bacteraemia, Convulsion, Pyrexia
on May 03, 2010 Male patient from UNITED STATES , child 11 years of age, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient had the following side effects: bacteraemia, convulsion, pyrexia. Benefix dosage: . Patient was hospitalized.

6714084-9 | Anaphylactic Reaction, Asthenia, Chest Discomfort, Dizziness, Dysgeusia, Dyspnoea, Fatigue, Headache
on Apr 28, 2010 Male patient from UNITED KINGDOM , weighting 205.0 lb, was diagnosed with haemorrhage, factor ix deficiency and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: anaphylactic reaction, asthenia, chest discomfort, dizziness (What is dizziness?), dysgeusia, dyspnoea, fatigue, headache (What is headache?). Benefix dosage: . Patient was hospitalized.

6690851-5 | Angina Pectoris
Patient was taking Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: angina pectoris on Sep 18, 2006 from DENMARK Additional patient health information: Male patient , weighting 125.7 lb, was diagnosed with factor ix deficiency and. Benefix dosage: 5000 Iu Q 24 Hours (87 Iu/kg). During the same period patient was treated with AMPICILLIN (View Ampicillin Review and Ampicillin Label ), NITROFURANTOIN (50 Mg Daily For 5 Months) (View Nitrofurantoin Review and Nitrofurantoin Label ).

6669424-6 | Erythema, Hypersensitivity, Restlessness, Urticaria
Adverse event was reported on Mar 26, 2010 by a Male patient taking Benefix (View Usage) (Dosage: On Demand) was diagnosed with factor ix deficiency and. Location: GERMANY , weighting 19.84 lb, Patient had the following side effects: erythema, hypersensitivity, restlessness, urticaria. During the same period patient was treated with ACETAMINOPHEN (On Demand) (View Acetaminophen Review and Acetaminophen Label ).

6558896-3 | Extradural Haematoma, Skull Fracture
on Jan 27, 2010 Male patient from GERMANY , child 3 years of age, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: extradural haematoma, skull fracture. Benefix dosage: . Patient was hospitalized.

6557460-X | Extradural Haematoma, Skull Fracture
on Jan 25, 2010 Male patient from GERMANY , child 3 years of age, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: extradural haematoma, skull fracture. Benefix dosage: . Patient was hospitalized.

6544009-0 | Anaphylactic Shock, Factor Ix Inhibition
Patient was taking Benefix (View Usage). Patient had the following side effects: anaphylactic shock, factor ix inhibition on Jan 12, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 22.05 lb, was diagnosed with factor ix deficiency and. Benefix dosage: Some Part Of A Dose (usual Dose 900u) In The Emergency Room; Vial Strength 250 Iu. Patient was hospitalized.

6481170-0 | Basal Cell Carcinoma, Inguinal Hernia
Adverse event was reported on Dec 03, 2009 by a Male patient taking Benefix (View Usage) (Dosage: ) was diagnosed with factor ix deficiency and. Location: GERMANY , 61 years of age, weighting 165.3 lb, After Benefix was administered, patient had the following side effects: basal cell carcinoma, inguinal hernia.

6481167-0 | Myocardial Infarction
on Dec 03, 2009 Male patient from GERMANY , 64 years of age, weighting 165.3 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction. Benefix dosage: 3000 Iu 2x Per Week.

6480843-3 | Myocardial Infarction
on Dec 01, 2009 Male patient from GERMANY , 64 years of age, weighting 165.3 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient had the following side effects: myocardial infarction. Benefix dosage: 3000 Iu 2x Per Week.

6436643-3 | Device Related Infection
Patient was taking Benefix (View Usage). After Benefix was administered, patient had the following side effects: device related infection on Nov 10, 2009 from GERMANY Additional patient health information: Male patient , weighting 19.84 lb, was diagnosed with factor ix deficiency and. Benefix dosage: Initial Dose Of 500 Iu. Patient was hospitalized.

6424061-3 | Dental Caries, Periodontitis
Adverse event was reported on Oct 29, 2009 by a Female patient taking Benefix (View Usage) (Dosage: ) was diagnosed with factor ix deficiency and. Location: GERMANY , 32 years of age, weighting 145.5 lb, Patient experienced the following unwanted or unexpected effects: dental caries, periodontitis. During the same period patient was treated with NORVIR (View Norvir Review and Norvir Label ), PREZISTA (View Prezista Review and Prezista Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), TAMSULOSIN HYDROCHLORIDE (View Tamsulosin Hydrochloride Review and Tamsulosin Hydrochloride Label ). Patient was hospitalized.

6419964-X | Dental Caries, Periodontitis
on Oct 26, 2009 Female patient from GERMANY , 32 years of age, weighting 145.5 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient had the following side effects: dental caries, periodontitis. Benefix dosage: . During the same period patient was treated with NORVIR (View Norvir Review and Norvir Label ), PREZISTA (View Prezista Review and Prezista Label ), PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), TAMSULOSIN HYDROCHLORIDE (View Tamsulosin Hydrochloride Review and Tamsulosin Hydrochloride Label ). Patient was hospitalized.

6419963-8 | Basal Cell Carcinoma, Inguinal Hernia
on Oct 23, 2009 Male patient from GERMANY , 61 years of age, weighting 165.3 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: basal cell carcinoma, inguinal hernia. Benefix dosage: .

6416686-6 | Myocardial Infarction
Patient was taking Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction on Oct 23, 2009 from GERMANY Additional patient health information: Male patient , 64 years of age, weighting 165.3 lb, was diagnosed with factor ix deficiency and. Benefix dosage: .

6397704-0 | Hip Arthroplasty
Adverse event was reported on Oct 12, 2009 by a Male patient taking Benefix (View Usage) (Dosage: ) was diagnosed with factor ix deficiency and. Location: BELGIUM , weighting 229.3 lb, Patient had the following side effects: hip arthroplasty. Patient was hospitalized.

6392301-5 | Abdominal Pain, Chest Pain, Dizziness, Dyspnoea, Hot Flush, Hypersensitivity, Malaise
on Sep 29, 2009 Male patient from UNITED KINGDOM , weighting 184.9 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), chest pain (What is chest pain?), dizziness (What is dizziness?), dyspnoea, hot flush, hypersensitivity, malaise. Benefix dosage: .

6379693-8 | Coagulation Factor Ix Level Decreased
on Sep 21, 2009 Male patient from GERMANY , weighting 74.08 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: coagulation factor ix level decreased. Benefix dosage: .

6375594-X | Deep Vein Thrombosis
Patient was taking Benefix (View Usage). Patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?) on Aug 20, 2009 from BELGIUM Additional patient health information: Male patient , 71 years of age, weighting 229.3 lb, was diagnosed with factor ix deficiency, surgery (What is surgery?) and. Benefix dosage: Fix Maintained At About 80% Until Day 4 Post-op.

6371715-3 | Coagulation Factor Ix Level Decreased
Adverse event was reported on Sep 17, 2009 by a Male patient taking Benefix (View Usage) (Dosage: 50 - 68 U/kg On Demand) was diagnosed with factor ix deficiency and. Location: SPAIN , weighting 127.9 lb, After Benefix was administered, patient had the following side effects: coagulation factor ix level decreased.

6347500-5 | Coagulation Factor Ix Level Decreased
on Aug 31, 2009 Male patient from GERMANY , child 9 years of age, weighting 74.08 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: coagulation factor ix level decreased. Benefix dosage: .

6346148-6 | Haemarthrosis, Underdose
on Sep 02, 2009 Male patient from SWITZERLAND , 42 years of age, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient had the following side effects: haemarthrosis, underdose. Benefix dosage: .

6346147-4 | Haemarthrosis, Underdose
Patient was taking Benefix (View Usage). After Benefix was administered, patient had the following side effects: haemarthrosis, underdose on Sep 02, 2009 from SWITZERLAND Additional patient health information: Male patient , 46 years of age, was diagnosed with factor ix deficiency and. Benefix dosage: .

6336992-3 | Haemarthrosis
Adverse event was reported on Aug 28, 2009 by a Male patient taking Benefix (View Usage) (Dosage: ) was diagnosed with factor ix deficiency and. Location: NETHERLANDS , weighting 33.07 lb, Patient experienced the following unwanted or unexpected effects: haemarthrosis.

6318117-3 | Muscle Haemorrhage, Traumatic Haematoma
on Aug 18, 2009 Male patient from FRANCE , weighting 176.4 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient had the following side effects: muscle haemorrhage, traumatic haematoma. Benefix dosage: . During the same period patient was treated with NORVIR (View Norvir Review and Norvir Label ), TRUVADA (View Truvada Review and Truvada Label ), INVIRASE (View Invirase Review and Invirase Label ).

6282234-7 | Factor Ix Inhibition
on Jul 13, 2009 Male patient from UNITED STATES , weighting 30.03 lb, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: factor ix inhibition. Benefix dosage: .

6278306-3 | Anaphylactic Shock, Factor Ix Inhibition
Patient was taking Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, factor ix inhibition on Jul 15, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 22.05 lb, was diagnosed with factor ix deficiency and. Benefix dosage: Some Part Of A Dose (usual Dose 900u) In The Emergency Room; Vial Strength 250 Iu. Patient was hospitalized.

6269270-1 | Catheter Related Infection, Staphylococcal Bacteraemia, Staphylococcal Infection
Adverse event was reported on Jul 07, 2009 by a Male patient taking Benefix (View Usage) (Dosage: ) was diagnosed with haemophilia, haemorrhage, pain (What is pain?), epistaxis and. Location: UNITED STATES , weighting 195.8 lb, Patient had the following side effects: catheter related infection, staphylococcal bacteraemia, staphylococcal infection (What is staphylococcal infection?). During the same period patient was treated with VICODIN (1 Tablet Every 4-6 Hours As Need For Pain) (View Vicodin Review and Vicodin Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), NEXIUM (View Nexium Review and Nexium Label ), AMICAR (500mg Tablets, 5 Tablets Every 4 Hours For Nosebleeds) (View Amicar Review and Amicar Label ), ZITHROMAX (600mg- 2 Tablets Weekly On Saturday) (View Zithromax Review and Zithromax Label ), DIOVAN HCT (80-12.5mg Daily) (View Diovan Hct Review and Diovan Hct Label ). Patient was hospitalized.

6262270-7 | Haemarthrosis, Underdose
on Jul 06, 2009 Male patient from SWITZERLAND , 42 years of age, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). After Benefix was administered, patient had the following side effects: haemarthrosis, underdose. Benefix dosage: .

6262268-9 | Haemarthrosis, Underdose
on Jul 06, 2009 Male patient from SWITZERLAND , 46 years of age, was diagnosed with factor ix deficiency and was treated with Benefix (View Usage). Patient experienced the following unwanted or unexpected effects: haemarthrosis, underdose. Benefix dosage: .

6261064-6 | Migraine With Aura
Patient was taking Benefix (View Usage). Patient had the following side effects: migraine with aura on Jul 02, 2009 from UNITED STATES Additional patient health information: Male patient , 32 years of age, was diagnosed with factor ix deficiency and. Benefix dosage: .

Showing 1-50 of 182  Next Page  >


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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 Benefix 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 Benefix quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Benefix 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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Benefix Reactions
Abnormal Sensation In Eye
Anaphylactic Reaction
Anaphylactoid Reaction
Anti Factor Ix Antibody Positive
Back PainWhat is Back pain?
Bacteraemia
Catheter Site Haemorrhage
Chest Discomfort
Coagulation Factor Ix Level Decreased
Cold Sweat
Convulsion
Cough
DizzinessWhat is Dizziness?
Dyspnoea
Eye Oedema
Factor Ix Inhibition
Flushing
Formication
Haemarthrosis
Haemorrhage
Hypersensitivity
Hypotension
Muscle Haemorrhage
NauseaWhat is Nausea?
Pruritus
Pyrexia
Respiratory Distress
Tremor
Urticaria
Vomiting
Benefix 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 Benefix 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!