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Summary

FDA Adverse Reports: 2. View All

Nadroparin FDA safety alerts: No

Reported hospitalizations: 1

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

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6554380-1 | Haematoma Evacuation, Haemoglobin Decreased, Haemorrhage, Heparin-induced Thrombocytopenia, Thoracic Operation
on Jan 18, 2010 Female patient from GERMANY , 77 years of age, weighting 154.3 lb, was treated with Nadroparin (View Usage). Patient experienced the following unwanted or unexpected effects: haematoma evacuation, haemoglobin decreased, haemorrhage, heparin-induced thrombocytopenia, thoracic operation. Nadroparin dosage: .7ml Per Day. 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 ).

4758796-5 | Leukocytoclastic Vasculitis
Patient was taking Nadroparin (View Usage). Patient had the following side effects: leukocytoclastic vasculitis on Aug 26, 2005 from SWITZERLAND Additional patient health information: Male patient , 73 years of age, . Nadroparin dosage: . During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ), SODIUM CHLORIDE (View Sodium Chloride Review and Sodium Chloride Label ), THIAMINE HYDROCHLORIDE (View Thiamine Hydrochloride Review and Thiamine Hydrochloride Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), PHYTONADIONE (View Phytonadione Review and Phytonadione Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), FOLIC ACID (View Folic Acid Review and Folic Acid 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 Nadroparin 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 Nadroparin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Nadroparin 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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During the same period patient was treated with TINZAPARIN SODIUM (View Tinzaparin Sodium Review and Tinzaparin Sodium Label ), NADROPARIN CALCIUM (View Nadroparin Calcium ...<<<<

... Acetaminophen Review and Acetaminophen Label ), SODIUM POLYSTYRENE SULFONATE (View Sodium Polystyrene Sulfonate Review and Sodium Polystyrene Sulfonate Label ), NADROPARIN ...<<<<

... Morphine Sulfate Review and Morphine Sulfate Label ), ZOCOR (View Zocor Review and Zocor Label ), NADROPARIN CALCIUM (View Nadroparin Calcium Review and Nadroparin Calcium ...<<<<

During the same period patient was treated with TINZAPARIN SODIUM (View Tinzaparin Sodium Review and Tinzaparin Sodium Label ), NADROPARIN CALCIUM (View Nadroparin Calcium ...<<<<

During the same period patient was treated with PREDNISOLONE (NGX) (0.8 Mg/kg Bodyweight/day) (View Prednisolone (ngx) Review and Prednisolone (ngx) Label ), NADROPARIN ...<<<<

During the same period patient was treated with ENALAPRIL MALEATE (20 Mg X Day) (View Enalapril Maleate Review and Enalapril Maleate Label ), NADROPARIN CALCIUM (View ...<<<<

... LINCOMYCIN (LINCOMYCIN) (View Lincomycin (lincomycin) Review and Lincomycin (lincomycin) Label ), NADROPARIN CALCIUM (NADROPARIN CALCIUM) (View Nadroparin Calcium ...<<<<

... Calcium Review and Carbaspirin Calcium Label ), CITALOPRAM (View Citalopram Review and Citalopram Label ), NADROPARIN CALCIUM (View Nadroparin Calcium Review and Nadroparin ...<<<<

... enalapril Maleat Review and Enalapril Maleate (enalapril Maleat Label ), NADROPARIN (NADROPARIN) (Weight-adjusted Dose Of 2 X0 ...<<<<

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

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Nadroparin Reactions
Haematoma Evacuation
Haemoglobin Decreased
Haemorrhage
Heparin-induced Thrombocytopenia
Leukocytoclastic Vasculitis
Thoracic Operation
Nadroparin 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 Nadroparin 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!