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Fraxiparin adverse events reported to FDA.

Have You Experienced unusual Fraxiparin symptoms? PatientsVille.com collects and analyzes Fraxiparin side effect and adverse reports submitted by Fraxiparin users, such as .

Summary

FDA Adverse Reports: 10. View All

Fraxiparin FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 9

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

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6911055-4 | Abortion, Heparin-induced Thrombocytopenia
on Aug 02, 2010 Female patient from GERMANY , 34 years of age, weighting 132.3 lb, was treated with Fraxiparin (View Usage). Patient experienced the following unwanted or unexpected effects: abortion (What is abortion?), heparin-induced thrombocytopenia. Fraxiparin dosage: . During the same period patient was treated with ARIXTRA (7.5mg Per Day) (View Arixtra Review and Arixtra Label ).

6661202-7 | Premature Baby
Patient was taking Fraxiparin (View Usage). Patient had the following side effects: premature baby on Mar 25, 2010 from GERMANY Additional patient health information: Female patient , 31 years of age, weighting 143.3 lb, was diagnosed with thrombosis prophylaxis and. Fraxiparin dosage: .6ml Per Day. During the same period patient was treated with ARIXTRA (2.5mg Per Day) (View Arixtra Review and Arixtra Label ), FRAGMIN (View Fragmin Review and Fragmin Label ).

6554381-3 | Bladder Tamponade, Haematuria, Heparin-induced Thrombocytopenia
Adverse event was reported on Jan 18, 2010 by a Female patient taking Fraxiparin (View Usage) (Dosage: .8ml Per Day) was diagnosed with prophylaxis and. Location: GERMANY , 78 years of age, weighting 174.2 lb, After Fraxiparin was administered, patient had the following side effects: bladder tamponade, haematuria, heparin-induced thrombocytopenia. During the same period patient was treated with FONDAPARINUX SODIUM (7.5mg Per Day) (View Fondaparinux Sodium Review and Fondaparinux Sodium Label ), UNFRACTIONATED HEPARIN (View Unfractionated Heparin Review and Unfractionated Heparin Label ), PHENPROCOUMON (View Phenprocoumon Review and Phenprocoumon Label ).

6332805-4 | Cerebrovascular Accident
on Aug 24, 2009 Female patient from GERMANY , 73 years of age, was diagnosed with thrombosis prophylaxis and was treated with Fraxiparin (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident. Fraxiparin dosage: . During the same period patient was treated with ARIXTRA (View Arixtra Review and Arixtra Label ), ACETYLCYSTEINE (View Acetylcysteine Review and Acetylcysteine Label ), FORMOTEROL POWDER (View Formoterol Powder Review and Formoterol Powder Label ), ARCOXIA (View Arcoxia Review and Arcoxia Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ).


6173573-9 | Cerebrovascular Accident
on Apr 29, 2009 Female patient from GERMANY , 73 years of age, was diagnosed with thrombosis prophylaxis and was treated with Fraxiparin (View Usage). Patient had the following side effects: cerebrovascular accident. Fraxiparin dosage: . During the same period patient was treated with ARIXTRA (View Arixtra Review and Arixtra Label ), ACETYLCYSTEINE (View Acetylcysteine Review and Acetylcysteine Label ), FORMOTEROL POWDER (View Formoterol Powder Review and Formoterol Powder Label ), ARCOXIA (View Arcoxia Review and Arcoxia Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ).

5848223-9 | Cardiovascular Disorder, Excoriation, Haemorrhage, Hypertension, Intra-abdominal Haemorrhage, Miosis, Somnolence
Patient was taking Fraxiparin (View Usage). After Fraxiparin was administered, patient had the following side effects: cardiovascular disorder, excoriation, haemorrhage, hypertension, intra-abdominal haemorrhage, miosis, somnolence on Aug 08, 2008 from GERMANY Additional patient health information: Male patient , 74 years of age, weighting 209.4 lb, . Fraxiparin dosage: 1ml See Dosage Text. During the same period patient was treated with LEXOTANIL (View Lexotanil Review and Lexotanil Label ), MARCUMAR (View Marcumar Review and Marcumar Label ), NEUROCIL (50mg Per Day) (View Neurocil Review and Neurocil Label ), SEROXAT (View Seroxat Review and Seroxat Label ), VITAMIN K TAB (View Vitamin K Tab Review and Vitamin K Tab Label ), DALMADORM (View Dalmadorm Review and Dalmadorm Label ). Patient was hospitalized.

5474808-8 | Thrombocythaemia
Adverse event was reported on Oct 01, 2007 by a Female patient taking Fraxiparin (View Usage) (Dosage: .4ml Per Day) was diagnosed with cervix cancer metastatic and. Location: GERMANY , 41 years of age, weighting 119.0 lb, Patient experienced the following unwanted or unexpected effects: thrombocythaemia. During the same period patient was treated with TOPOTECAN (1.21mg As Directed) (View Topotecan Review and Topotecan Label ), CISPLATIN (80.5mg Per Day) (View Cisplatin Review and Cisplatin Label ), NEORECORMON (30000iu As Directed) (View Neorecormon Review and Neorecormon Label ).

5315816-7 | Dyspnoea, Feeling Hot, Injection Site Erythema, Injection Site Vesicles, Rash, Throat Tightness
on Apr 26, 2007 Female patient from CZECH REPUBLIC , 39 years of age, was diagnosed with venous thrombosis, thrombosis prophylaxis and was treated with Fraxiparin (View Usage). Patient had the following side effects: dyspnoea, feeling hot, injection site erythema, injection site vesicles, rash (What is rash?), throat tightness. Fraxiparin dosage: . During the same period patient was treated with ARIXTRA (View Arixtra Review and Arixtra Label ), LETROX (View Letrox Review and Letrox Label ). Patient was hospitalized.

4644141-2 | Erythema Multiforme
on Mar 28, 2005 Female patient from , 66 years of age, was treated with Fraxiparin (View Usage). After Fraxiparin was administered, patient had the following side effects: erythema multiforme. Fraxiparin dosage: . During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), TROXERUTIN (View Troxerutin Review and Troxerutin Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

4642386-9 | Erythema Multiforme
Patient was taking Fraxiparin (View Usage). Patient experienced the following unwanted or unexpected effects: erythema multiforme on Mar 28, 2005 from Additional patient health information: Female patient , 66 years of age, . Fraxiparin dosage: . During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), TROXERUTIN (View Troxerutin Review and Troxerutin Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole 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 Fraxiparin 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 Fraxiparin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fraxiparin 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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Fraxiparine Side Effects - Complete Patient's Guide | User Reviews: Male patient, 43 years of age, weighting 132.3 |Eaching|Licht Headed|Augumentin

fraxiparine Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: fungizone Episodes: 1: Diagnosed with major depression ...

)During the same period patient was treated with AUGMENTIN (2.2 G Tid Iv) (View Augmentin Review and Augmentin Label ), FRAXIPARINE (View Fraxiparine Review and Fraxiparine ...

... Kaletra Label ), COMBIVIR (View Combivir Review and Combivir Label ), RETROVIR (View Retrovir Review and Retrovir Label ), FRAXIPARIN (View Fraxiparin Review and Fraxiparin ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

During the same period patient was treated with FRAXIPARINE (0.4 Ml, Qd) (View Fraxiparine Review and Fraxiparine Label ), DUPHALAC (10 G, 6qd) (View Duphalac Review and ...

Fraxiparine Side Effects Fraxiparine Side ... During the same period patient was treated with LEXAPRO (View Lexapro Review and Lexapro Label ), ELEVIT (View Elevit Review ...

... Total Daily Dose: 1800 Mg Unit Dose: 600 Mg) (View Ibuprofen Review and Ibuprofen Label ), FRAXIPARIN (Total Daily Dose: 2850 Iu) (View Fraxiparin Review and Fraxiparin ...

... Clopidogrel Label ), HEPARIN (1000 Mg, Units/hr, Intravenous) (View Heparin Review and Heparin Label ), FRAXIPARIN (NADROPARIN CALCIUM) (0.40 Units, Qd) (View Fraxiparin ...

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Fraxiparin Reactions
AbortionWhat is Abortion?
Bladder Tamponade
Cardiovascular Disorder
Cerebrovascular Accident
Dyspnoea
Erythema Multiforme
Excoriation
Feeling Hot
Haematuria
Haemorrhage
Heparin-induced Thrombocytopenia
Hypertension
Injection Site Erythema
Injection Site Vesicles
Intra-abdominal Haemorrhage
Miosis
Premature Baby
RashWhat is Rash?
Somnolence
Throat Tightness
Thrombocythaemia
Fraxiparin 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 Fraxiparin 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!