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Atelec adverse events reported to FDA.

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Summary

FDA Adverse Reports: 9. View All

Atelec FDA safety alerts: No

Reported deaths: 5

Reported hospitalizations: 4

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

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6474797-3 | Acidosis, Blood Creatinine Increased, Bradyarrhythmia, Cardiac Failure, Decreased Appetite, Gait Disturbance, Hyperkalaemia
on Sep 02, 2009 Male patient from JAPAN , 76 years of age, was diagnosed with ill-defined disorder, hypertension, cardiac failure and was treated with Atelec (View Usage). Patient experienced the following unwanted or unexpected effects: acidosis, blood creatinine increased, bradyarrhythmia, cardiac failure, decreased appetite, gait disturbance, hyperkalaemia. Atelec dosage: . During the same period patient was treated with COVERSYL (Daily Dose: 8 Milligram(s)) (View Coversyl Review and Coversyl Label ), SPIRONOLACTONE (Daily Dose: 50 Milligram(s)) (View Spironolactone Review and Spironolactone Label ), LASIX (View Lasix Review and Lasix Label ), NATEGLINIDE (View Nateglinide Review and Nateglinide Label ), CILNIDIPINE (Daily Dose: 20 Milligram(s)) (View Cilnidipine Review and Cilnidipine Label ), GLUCOBAY (View Glucobay Review and Glucobay Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

5405608-2 | Subarachnoid Haemorrhage
Patient was taking Atelec (View Usage). Patient had the following side effects: subarachnoid haemorrhage on Aug 01, 2007 from JAPAN Additional patient health information: Male patient , 56 years of age, weighting 167.6 lb, was diagnosed with hypertension and. Atelec dosage: . During the same period patient was treated with DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ), DIALYSIS (View Dialysis Review and Dialysis Label ), PHARLODINE (View Pharlodine Review and Pharlodine Label ), STOGAR (View Stogar Review and Stogar Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ), OXAROL (View Oxarol Review and Oxarol Label ).

5387331-6 | Subarachnoid Haemorrhage
Adverse event was reported on Jul 10, 2007 by a Male patient taking Atelec (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 56 years of age, weighting 167.6 lb, After Atelec was administered, patient had the following side effects: subarachnoid haemorrhage. During the same period patient was treated with DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ), DIALYSIS (View Dialysis Review and Dialysis Label ), PHARLODINE (View Pharlodine Review and Pharlodine Label ), STOGAR (View Stogar Review and Stogar Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ), OXAROL (View Oxarol Review and Oxarol Label ).

5327189-4 | Subarachnoid Haemorrhage
on May 11, 2007 Male patient from JAPAN , 56 years of age, weighting 167.6 lb, was diagnosed with hypertension and was treated with Atelec (View Usage). Patient experienced the following unwanted or unexpected effects: subarachnoid haemorrhage. Atelec dosage: . During the same period patient was treated with DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ), DIALYSIS (View Dialysis Review and Dialysis Label ).


5133437-6 | Blood Creatinine Increased, Bradyarrhythmia, Cardiac Failure, Hyperkalaemia
on Sep 27, 2006 Male patient from JAPAN , 76 years of age, was diagnosed with ill-defined disorder, hypertension, cardiac failure and was treated with Atelec (View Usage). Patient had the following side effects: blood creatinine increased, bradyarrhythmia, cardiac failure, hyperkalaemia. Atelec dosage: . During the same period patient was treated with PERINDOPRIL ERBUMINE (Daily Dose: 8 Milligram(s)) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), LASIX (View Lasix Review and Lasix Label ), SPIRONOLACTONE (Daily Dose: 50 Milligram(s)) (View Spironolactone Review and Spironolactone Label ), NATEGLINIDE (View Nateglinide Review and Nateglinide Label ), GLUCOBAY (View Glucobay Review and Glucobay Label ). Patient was hospitalized.

5017716-9 | Cardio-respiratory Arrest
Patient was taking Atelec (View Usage). After Atelec was administered, patient had the following side effects: cardio-respiratory arrest on Feb 08, 2006 from JAPAN Additional patient health information: Male patient , 56 years of age, was diagnosed with hypertension and. Atelec dosage: 5 Mg, Unk. During the same period patient was treated with SELECTOL (100 Mg, Unk) (View Selectol Review and Selectol Label ), ALDOMET (750 Mg, Unk) (View Aldomet Review and Aldomet Label ), DIOVAN (40 Mg, Qd) (View Diovan Review and Diovan Label ).

4909828-2 |
Adverse event was reported on Feb 08, 2006 by a Male patient taking Atelec (View Usage) (Dosage: 5 Mg, Unk) was diagnosed with hypertension and. Location: JAPAN , 56 years of age, . During the same period patient was treated with SELECTOL (100 Mg, Unk) (View Selectol Review and Selectol Label ), ALDOMET (750 Mg, Unk) (View Aldomet Review and Aldomet Label ), DIOVAN (40 Mg, Qd) (View Diovan Review and Diovan Label ).

4661739-6 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bile Duct Stone, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Amylase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gallstones In Bile Duct Removal
on Mar 31, 2005 Male patient from , 79 years of age, was diagnosed with hypertension and was treated with Atelec (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bile duct stone, bilirubin conjugated increased, blood alkaline phosphatase increased, blood amylase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gallstones in bile duct removal. Atelec dosage: Unk, Unk. During the same period patient was treated with HARNAL (Unk, Unk) (View Harnal Review and Harnal Label ), DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan Label ). Patient was hospitalized.

4647627-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bile Duct Stone, Blood Bilirubin Increased, Gallstones In Bile Duct Removal, Liver Function Test Abnormal
on Mar 31, 2005 Male patient from , 79 years of age, was diagnosed with hypertension and was treated with Atelec (View Usage). After Atelec was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bile duct stone, blood bilirubin increased, gallstones in bile duct removal, liver function test abnormal. Atelec dosage: Unk, Unk. During the same period patient was treated with HARNAL (Unk, Unk) (View Harnal Review and Harnal Label ), DIOVAN (80 Mg, Qd) (View Diovan Review and Diovan 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 Atelec 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 Atelec quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Atelec 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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Atelec Reactions
Acidosis
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Bile Duct Stone
Bilirubin Conjugated Increased
Blood Alkaline Phosphatase Increased
Blood Amylase Increased
Blood Bilirubin Increased
Blood Creatinine Increased
Blood Lactate Dehydrogenase Increased
Bradyarrhythmia
Cardiac Failure
Cardio-respiratory Arrest
Decreased Appetite
Gait Disturbance
Gallstones In Bile Duct Removal
Hyperkalaemia
Liver Function Test Abnormal
Subarachnoid Haemorrhage
Sudden Death
Atelec 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 Atelec 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!