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Fraxiparine adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 11. View All

Fraxiparine FDA safety alerts: No

Reported hospitalizations: 9

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

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6867194-X | Ischaemic Stroke, Neurological Symptom, Pain
on Jul 07, 2010 Male patient from BELGIUM , 43 years of age, weighting 132.3 lb, was diagnosed with pain (What is pain?) and was treated with Fraxiparine (View Usage). Patient experienced the following unwanted or unexpected effects: ischaemic stroke, neurological symptom, pain (What is pain?). Fraxiparine dosage: . During the same period patient was treated with SUMATRIPTAN (View Sumatriptan Review and Sumatriptan Label ).

6828052-X | Ischaemic Stroke, Neurological Symptom, Pain, Vasospasm
Patient was taking Fraxiparine (View Usage). Patient had the following side effects: ischaemic stroke, neurological symptom, pain (What is pain?), vasospasm on Jun 29, 2010 from BELGIUM Additional patient health information: Male patient , 43 years of age, weighting 132.3 lb, was diagnosed with carotid artery thrombosis, pain (What is pain?) and. Fraxiparine dosage: . During the same period patient was treated with SUMATRIPTAN SUCCINATE (View Sumatriptan Succinate Review and Sumatriptan Succinate Label ).

5993970-1 | Dyspnoea, Hypersensitivity, Pruritus, Rash
Adverse event was reported on Dec 03, 2008 by a Female patient taking Fraxiparine (View Usage) (Dosage: ) was diagnosed with deep vein thrombosis (What is deep vein thrombosis?) and. Location: PALESTINIAN TERRITORY, OCCUPIED , 27 years of age, After Fraxiparine was administered, patient had the following side effects: dyspnoea, hypersensitivity, pruritus, rash (What is rash?). During the same period patient was treated with CEFUROXIME (View Cefuroxime Review and Cefuroxime Label ). Patient was hospitalized.

5479653-5 | Apallic Syndrome, Aphasia, Cerebral Haematoma, Cerebral Haemorrhage, Gaze Palsy, Haemoglobin Decreased, Hemiplegia, Pyrexia
on Sep 26, 2007 Female patient from FRANCE , 67 years of age, weighting 154.3 lb, was diagnosed with cerebrovascular accident prophylaxis, depression (What is depression?), anaemia, neuralgia and was treated with Fraxiparine (View Usage). Patient experienced the following unwanted or unexpected effects: apallic syndrome, aphasia (What is aphasia?), cerebral haematoma, cerebral haemorrhage, gaze palsy, haemoglobin decreased, hemiplegia, pyrexia. Fraxiparine dosage: .3ml Per Day. During the same period patient was treated with PAROXETINE (20mg Per Day) (View Paroxetine Review and Paroxetine Label ), TARDYFERON (160mg Per Day) (View Tardyferon Review and Tardyferon Label ), RIVOTRIL (5drop At Night) (View Rivotril Review and Rivotril Label ), DAFALGAN (1000mg Three Times Per Day) (View Dafalgan Review and Dafalgan Label ), INEXIUM (40mg At Night) (View Inexium Review and Inexium Label ), PRIMPERAN (3sp Three Times Per Day) (View Primperan Review and Primperan Label ), DIFFU K (3unit Per Day) (View Diffu K Review and Diffu K Label ). Patient was hospitalized.


5367043-5 | Eosinophilia, Pruritus
on Jun 08, 2007 Male patient from FRANCE , 68 years of age, was treated with Fraxiparine (View Usage). Patient had the following side effects: eosinophilia, pruritus. Fraxiparine dosage: . During the same period patient was treated with RANIPLEX (50mg Per Day) (View Raniplex Review and Raniplex Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), SPASFON (View Spasfon Review and Spasfon Label ). Patient was hospitalized.

5101426-3 | Apallic Syndrome, Cerebral Haematoma, Cerebral Haemorrhage, Gaze Palsy, Hemiplegia, Pyrexia, Sensory Loss
Patient was taking Fraxiparine (View Usage). After Fraxiparine was administered, patient had the following side effects: apallic syndrome, cerebral haematoma, cerebral haemorrhage, gaze palsy, hemiplegia, pyrexia, sensory loss on Aug 30, 2006 from FRANCE Additional patient health information: Female patient , 67 years of age, weighting 154.3 lb, was diagnosed with cerebrovascular accident prophylaxis, neuralgia and. Fraxiparine dosage: .3ml Per Day. During the same period patient was treated with DEROXAT (20mg Per Day) (View Deroxat Review and Deroxat Label ), NEXIUM (40mg At Night) (View Nexium Review and Nexium Label ), TARDYFERON (160mg Per Day) (View Tardyferon Review and Tardyferon Label ), RIVOTRIL (5drop At Night) (View Rivotril Review and Rivotril Label ), DAFALGAN (1000mg Three Times Per Day) (View Dafalgan Review and Dafalgan Label ), PRIMPERAN TAB (3sp Three Times Per Day) (View Primperan Tab Review and Primperan Tab Label ), DIFFU K (3unit Per Day) (View Diffu K Review and Diffu K Label ). Patient was hospitalized.

4979204-5 | Gastrointestinal Haemorrhage
Adverse event was reported on Apr 10, 2006 by a Female patient taking Fraxiparine (View Usage) (Dosage: 2850iu Per Day) was diagnosed with femoral neck fracture and. Location: SPAIN , 82 years of age, Patient experienced the following unwanted or unexpected effects: gastrointestinal haemorrhage. During the same period patient was treated with ZINNAT (500mg Per Day) (View Zinnat Review and Zinnat Label ), NEOBRUFEN (600mg Per Day) (View Neobrufen Review and Neobrufen Label ), SINEMET (1tab Three Times Per Day) (View Sinemet Review and Sinemet Label ), PANTOPRAZOL (View Pantoprazol Review and Pantoprazol Label ). Patient was hospitalized.

4973005-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Headache, Hepatocellular Damage, Hyperthermia, Lung Disorder, Neck Pain
on Apr 05, 2006 Female patient from FRANCE , 59 years of age, was diagnosed with thrombosis prophylaxis, chest pain (What is chest pain?), lung disorder, hypercholesterolaemia and was treated with Fraxiparine (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, headache (What is headache?), hepatocellular damage, hyperthermia, lung disorder, neck pain. Fraxiparine dosage: 10000iuax Per Day. During the same period patient was treated with PERFALGAN (3g Per Day) (View Perfalgan Review and Perfalgan Label ), PROPOFOL (6tab Per Day) (View Propofol Review and Propofol Label ), AUGMENTIN '125' (3g Per Day) (View Augmentin '125' Review and Augmentin '125' Label ), ZOCOR (10mg Per Day) (View Zocor Review and Zocor Label ), LECTIL (16mg Per Day) (View Lectil Review and Lectil Label ). Patient was hospitalized.

4668988-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, C-reactive Protein Increased, Cholestasis, Gamma-glutamyltransferase Increased, Jaundice
on May 12, 2005 Male patient from , 65 years of age, was diagnosed with essential hypertension and was treated with Fraxiparine (View Usage). After Fraxiparine was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, c-reactive protein increased, cholestasis, gamma-glutamyltransferase increased, jaundice (What is jaundice?). Fraxiparine dosage: 1u Per Day. During the same period patient was treated with AVANDIA (View Avandia Review and Avandia Label ), FUROSEMIDE (40mg See Dosage Text) (View Furosemide Review and Furosemide Label ), PANTOPRAZOLE SODIUM (40mg Per Day) (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), PARACETAMOL (2tab Four Times Per Day) (View Paracetamol Review and Paracetamol Label ), CIPROFLOXACIN HYDROCHLORIDE (1tab Per Day) (View Ciprofloxacin Hydrochloride Review and Ciprofloxacin Hydrochloride Label ), METRONIDAZOLE (500mg Per Day) (View Metronidazole Review and Metronidazole Label ), PIPAMPERONE HYDROCHLORIDE (.5u Per Day) (View Pipamperone Hydrochloride Review and Pipamperone Hydrochloride Label ). Patient was hospitalized.

4658630-8 | Aphasia, Communication Disorder, Epilepsy, Facial Palsy, Somnolence
Patient was taking Fraxiparine (View Usage). Patient experienced the following unwanted or unexpected effects: aphasia (What is aphasia?), communication disorder, epilepsy (What is epilepsy?), facial palsy, somnolence on Apr 29, 2005 from Additional patient health information: Female patient , 64 years of age, weighting 185.2 lb, was diagnosed with ill-defined disorder, essential hypertension and. Fraxiparine dosage: .4ml Per Day. During the same period patient was treated with SEREVENT (2puff Per Day) (View Serevent Review and Serevent Label ), TAVANIC (500mg Per Day) (View Tavanic Review and Tavanic Label ), MOPRAL (20mg Per Day) (View Mopral Review and Mopral Label ), ALDACTAZINE (1tab Per Day) (View Aldactazine Review and Aldactazine Label ), RIFADIN (300mg Four Times Per Day) (View Rifadin Review and Rifadin Label ), DAFLON (View Daflon Review and Daflon Label ), DIAMICRON (1unit Per Day) (View Diamicron Review and Diamicron Label ). Patient was hospitalized.

4601630-4 | Haematuria, Tubulointerstitial Nephritis
Adverse event was reported on Aug 11, 2004 by a Male patient taking Fraxiparine (View Usage) (Dosage: ) was diagnosed with stress ulcer and. Location: , 13 years of age, weighting 132.3 lb, Patient had the following side effects: haematuria, tubulointerstitial nephritis. During the same period patient was treated with ZANTAC (View Zantac Review and Zantac Label ), CLAMOXYL (View Clamoxyl Review and Clamoxyl Label ), NIMBEX (View Nimbex Review and Nimbex Label ), TETANUS VACCINE (1 Per Day) (View Tetanus Vaccine Review and Tetanus Vaccine Label ), TRACRIUM (View Tracrium Review and Tracrium Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), IMMUNOGLOBULIN HUMAN ANTI TETANUS (1 Per Day) (View Immunoglobulin Human Anti-tetanus Review and Immunoglobulin Human Anti-tetanus 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 Fraxiparine 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 Fraxiparine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fraxiparine 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 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 FRAXIPARINE (0.4 Ml, Qd) (View Fraxiparine Review and Fraxiparine Label ), DUPHALAC (10 G, 6qd) (View Duphalac Review and ...

)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 ...

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 ...

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

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

... Importal Label ), NEXIUM (View Nexium Review and Nexium Label ), MORPHINE (View Morphine Review and Morphine Label ), FRAXIPARINE (View Fraxiparine Review and Fraxiparine Label ).

... day) (View Celebrex Review and Celebrex Label ), NEXIUM (40 Mg/day) (View Nexium Review and Nexium Label ), FRAXIPARINE (.16 Ml, Qd) (View Fraxiparine Review and Fraxiparine ...

During the same period patient was treated with FRAXIPARINE (1.6mg Per Day) (View Fraxiparine Review and Fraxiparine Label ), VENTOLIN (View Ventolin Review and Ventolin ...

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Fraxiparine Reactions
Alanine Aminotransferase Increased
Apallic Syndrome
AphasiaWhat is Aphasia?
Aspartate Aminotransferase Increased
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
C-reactive Protein Increased
Cerebral Haematoma
Cerebral Haemorrhage
Cholestasis
Communication Disorder
Dyspnoea
Eosinophilia
EpilepsyWhat is Epilepsy?
Facial Palsy
Gamma-glutamyltransferase Increased
Gastrointestinal Haemorrhage
Gaze Palsy
Haematuria
Haemoglobin Decreased
HeadacheWhat is Headache?
Hemiplegia
Hepatocellular Damage
Hypersensitivity
Hyperthermia
Ischaemic Stroke
Neurological Symptom
PainWhat is Pain?
Pruritus
Pyrexia
Fraxiparine 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 Fraxiparine 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!