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Calciparine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Calciparine FDA safety alerts: No

Reported hospitalizations: 3

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

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6981571-8 | Haematemesis, Melaena, Renal Failure Acute
on Aug 31, 2010 Male patient from FRANCE , 82 years of age, was diagnosed with lung infection and was treated with Calciparine (View Usage). Patient experienced the following unwanted or unexpected effects: haematemesis, melaena, renal failure acute. Calciparine dosage: . During the same period patient was treated with KARDEGIC (View Kardegic Review and Kardegic Label ), PLAVIX (View Plavix Review and Plavix Label ), TAVANIC (View Tavanic Review and Tavanic Label ), PRAXILENE (View Praxilene Review and Praxilene Label ), BUMEX (View Bumex Review and Bumex Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), ADVIL LIQUI GELS (View Advil Liqui-gels Review and Advil Liqui-gels Label ), ELISOR (View Elisor Review and Elisor Label ). Patient was hospitalized.

6766324-8 | Activated Partial Thromboplastin Time Prolonged, Haematocrit Decreased, Haemoglobin Decreased, Intra-abdominal Haemorrhage, Overdose, Renal Failure
Patient was taking Calciparine (View Usage). Patient had the following side effects: activated partial thromboplastin time prolonged, haematocrit decreased, haemoglobin decreased, intra-abdominal haemorrhage, overdose, renal failure on Jun 01, 2010 from FRANCE Additional patient health information: Female patient , 90 years of age, was diagnosed with deep vein thrombosis (What is deep vein thrombosis?), hypothyroidism and. Calciparine dosage: . During the same period patient was treated with KARDEGIC (View Kardegic Review and Kardegic Label ), LASIX (View Lasix Review and Lasix Label ), PREVISCAN (View Previscan Review and Previscan Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ).

5583211-1 | Leukopenia
Adverse event was reported on Dec 26, 2007 by a Female patient taking Calciparine (View Usage) (Dosage: 0.4 Ml) was diagnosed with bladder catheterisation, urinary tract infection (What is urinary tract infection?) and. Location: FRANCE , 89 years of age, After Calciparine was administered, patient had the following side effects: leukopenia. During the same period patient was treated with DEROXAT (Unk) (View Deroxat Review and Deroxat Label ), INIPOMP (Unk) (View Inipomp Review and Inipomp Label ), XATRAL (Unk) (View Xatral Review and Xatral Label ), EFFERALGAN CODEINE (6 Unit) (View Efferalgan Codeine Review and Efferalgan Codeine Label ), ROCEPHIN (1 G) (View Rocephin Review and Rocephin Label ). Patient was hospitalized.

4551981-7 | Condition Aggravated, Renal Cyst, Renal Failure Acute
on Dec 27, 2004 Male patient from , 87 years of age, was diagnosed with phlebitis, chronic lymphocytic leukaemia and was treated with Calciparine (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, renal cyst, renal failure acute. Calciparine dosage: 0.3 Ml Tid, Subcutaneous. During the same period patient was treated with XATRAL (ALFUZOSIN) TABLET (Oral) (View Xatral - (alfuzosin) - Tablet Review and Xatral - (alfuzosin) - Tablet Label ), KAYEXALATE (SODIUM POLYSTYRENE SULFONATE) POWDER 15 MG (View Kayexalate (sodium Polystyrene Sulfonate) - Powder - 15 Mg Review and Kayexalate (sodium Polystyrene Sulfonate) - Powder - 15 Mg Label ), CORTANCYL (PREDNISONE) TABLET 5MG (5 Mg Od, Oral) (View Cortancyl (prednisone) - Tablet - 5mg Review and Cortancyl (prednisone) - Tablet - 5mg Label ), FUROSEMIDE (20 Mg Od, Oral) (View Furosemide Review and Furosemide Label ), CHLORAMINOPHENE ^TECHNI PHARMA^ (CHLORAMBUCIL) CAPSULE 2 MG (2 Mg 3/week, Oral) (View Chloraminophene ^techni-pharma^ - (chlorambucil) - Capsule - 2 Mg Review and Chloraminophene ^techni-pharma^ - (chlorambucil) - Capsule - 2 Mg Label ), OMEPRAZOLE (20 Mg Od, Oral) (View Omeprazole Review and Omeprazole Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), FORLAX (MACROGOL) POWDER 10 G (Ig Tid) (View Forlax - (macrogol) - Powder - 10 G Review and Forlax - (macrogol) - Powder - 10 G 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 Calciparine 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 Calciparine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Calciparine 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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Calciparine Reactions
Activated Partial Thromboplastin Time Prolonged
Condition Aggravated
Haematemesis
Haematocrit Decreased
Haemoglobin Decreased
Intra-abdominal Haemorrhage
Leukopenia
Melaena
Overdose
Renal Cyst
Renal Failure
Renal Failure Acute
Calciparine 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 Calciparine 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!