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

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5908721-6 | Gastrointestinal Haemorrhage, Haemoptysis, Respiratory Tract Haemorrhage
on Oct 03, 2008 Male patient from JAPAN , 71 years of age, was diagnosed with thrombosis prophylaxis and was treated with Relifen (View Usage). Patient experienced the following unwanted or unexpected effects: gastrointestinal haemorrhage, haemoptysis, respiratory tract haemorrhage. Relifen dosage: 800mg Per Day. During the same period patient was treated with CALONAL (1800mg Per Day) (View Calonal Review and Calonal Label ), RABEPRAZOLE SODIUM (10mg Per Day) (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ), WARFARIN SODIUM (3mg Per Day) (View Warfarin Sodium Review and Warfarin Sodium Label ), THEO DUR (200mg Per Day) (View Theo-dur Review and Theo-dur Label ), THYRADIN (25mcg Per Day) (View Thyradin Review and Thyradin Label ), AMOBAN (15mg Per Day) (View Amoban Review and Amoban Label ), GABAPENTIN (300mg Per Day) (View Gabapentin Review and Gabapentin Label ).

5889621-7 | Gastrointestinal Haemorrhage, Haemoptysis, Respiratory Tract Haemorrhage
Patient was taking Relifen (View Usage). Patient had the following side effects: gastrointestinal haemorrhage, haemoptysis, respiratory tract haemorrhage on Sep 17, 2008 from JAPAN Additional patient health information: Male patient , 71 years of age, was diagnosed with thrombosis prophylaxis and. Relifen dosage: 800mg Per Day. During the same period patient was treated with CALONAL (1800mg Per Day) (View Calonal Review and Calonal Label ), RABEPRAZOLE SODIUM (10mg Per Day) (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ), WARFARIN SODIUM (3mg Per Day) (View Warfarin Sodium Review and Warfarin Sodium Label ), THEO DUR (200mg Per Day) (View Theo-dur Review and Theo-dur Label ), THYRADIN (25mcg Per Day) (View Thyradin Review and Thyradin Label ), AMOBAN (15mg Per Day) (View Amoban Review and Amoban Label ), GABAPENTIN (300mg Per Day) (View Gabapentin Review and Gabapentin Label ).

5865240-3 | Haemoptysis, International Normalised Ratio Increased, Melaena
Adverse event was reported on Aug 27, 2008 by a Male patient taking Relifen (View Usage) (Dosage: 800mg Per Day) was diagnosed with cancer pain and. Location: JAPAN , 71 years of age, After Relifen was administered, patient had the following side effects: haemoptysis, international normalised ratio increased, melaena. During the same period patient was treated with ACETAMINOPHEN (1800mg Per Day) (View Acetaminophen Review and Acetaminophen Label ), RABEPRAZOLE SODIUM (10mg Per Day) (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ), THEO DUR (200mg Per Day) (View Theo-dur Review and Theo-dur Label ), THYRADIN (25mcg Per Day) (View Thyradin Review and Thyradin Label ), AMOBAN (15mg Per Day) (View Amoban Review and Amoban Label ), GABAPENTIN (300mg Per Day) (View Gabapentin Review and Gabapentin Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), PURSENNID (12mg Per Day) (View Pursennid Review and Pursennid Label ).

5154004-4 | Blood Alkaline Phosphatase Increased, Blood Chloride Increased, Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Urea Increased, Diarrhoea, Face Oedema, Oedema Peripheral
on Jul 07, 2006 Male patient from JAPAN , 77 years of age, was treated with Relifen (View Usage). Patient experienced the following unwanted or unexpected effects: blood alkaline phosphatase increased, blood chloride increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, diarrhoea, face oedema, oedema peripheral. Relifen dosage: 400mg Per Day. During the same period patient was treated with EPERISONE HYDROCHLORIDE (150mg Per Day) (View Eperisone Hydrochloride Review and Eperisone Hydrochloride Label ), ALFACALCIDOL (.5mg Per Day) (View Alfacalcidol Review and Alfacalcidol Label ), CILOSTAZOL (200mg Per Day) (View Cilostazol Review and Cilostazol Label ), TAMSULOSIN HCL (.2mg Per Day) (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), OMEPRAZOLE (10mg Per Day) (View Omeprazole Review and Omeprazole Label ), MYONAL (150mg Per Day) (View Myonal Review and Myonal Label ).


5149262-6 | Blood Alkaline Phosphatase Increased, Blood Chloride Increased, Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Urea Increased, Diarrhoea, Face Oedema, Oedema Peripheral
on Jul 07, 2006 Male patient from JAPAN , 77 years of age, was treated with Relifen (View Usage). Patient had the following side effects: blood alkaline phosphatase increased, blood chloride increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, diarrhoea, face oedema, oedema peripheral. Relifen dosage: 400mg Per Day. During the same period patient was treated with EPERISONE HYDROCHLORIDE (150mg Per Day) (View Eperisone Hydrochloride Review and Eperisone Hydrochloride Label ), ALFACALCIDOL (.5mg Per Day) (View Alfacalcidol Review and Alfacalcidol Label ), CILOSTAZOL (200mg Per Day) (View Cilostazol Review and Cilostazol Label ), TAMSULOSIN HCL (.2mg Per Day) (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), OMEPRAZOLE (10mg Per Day) (View Omeprazole Review and Omeprazole Label ), MYONAL (150mg Per Day) (View Myonal Review and Myonal Label ).


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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 Relifen 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 Relifen quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Relifen 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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Relifen Reactions
Blood Alkaline Phosphatase Increased
Blood Chloride Increased
Blood Creatinine Increased
Blood Lactate Dehydrogenase Increased
Blood Urea Increased
Diarrhoea
Face Oedema
Gastrointestinal Haemorrhage
Haemoptysis
International Normalised Ratio Increased
Melaena
Oedema Peripheral
Respiratory Tract Haemorrhage
Relifen 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 Relifen 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!