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FDA Adverse Reports: 5. View All

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

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6074710-7 | Blood Amylase Increased
on Feb 04, 2009 Male patient from JAPAN , 78 years of age, weighting 110.2 lb, was diagnosed with acute coronary syndrome and was treated with Diart (View Usage). Patient experienced the following unwanted or unexpected effects: blood amylase increased. Diart dosage: Unk. During the same period patient was treated with ARTIST (Unk) (View Artist Review and Artist Label ), SIGMART (Unk) (View Sigmart Review and Sigmart Label ), GASTER (Unk) (View Gaster Review and Gaster Label ), ADALAT CC (Unk) (View Adalat Cc Review and Adalat Cc Label ), DIOVAN (Unk) (View Diovan Review and Diovan Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ), PLAVIX (300 Mg Once Followed By 75 Mg Daily) (View Plavix Review and Plavix Label ).

5344152-8 | Blood Glucose Increased, Glycosylated Haemoglobin Increased, Renal Impairment
Patient was taking Diart (View Usage). Patient had the following side effects: blood glucose increased, glycosylated haemoglobin increased, renal impairment on May 28, 2007 from JAPAN Additional patient health information: Male patient , weighting 135.9 lb, . Diart dosage: 45 Mg. During the same period patient was treated with MEILAX (2 Tablets) (View Meilax Review and Meilax Label ), AMOBAN (1 Tablet) (View Amoban Review and Amoban Label ), AZUCURENIN S (1.5 G) (View Azucurenin S Review and Azucurenin S Label ), NITOROL (3 Tablets) (View Nitorol Review and Nitorol Label ), COMELIAN (300 Mg) (View Comelian Review and Comelian Label ), TENAXIL (1 Mg) (View Tenaxil Review and Tenaxil Label ), DIACORT (90 Mg) (View Diacort Review and Diacort Label ).

5304819-4 | Blood Glucose Increased, Glycosylated Haemoglobin Increased, Renal Impairment
Adverse event was reported on Apr 13, 2007 by a Male patient taking Diart (View Usage) (Dosage: 45 Mg) . Location: JAPAN , weighting 135.9 lb, After Diart was administered, patient had the following side effects: blood glucose increased, glycosylated haemoglobin increased, renal impairment. During the same period patient was treated with MEILAX (2 Tablets) (View Meilax Review and Meilax Label ), AMOBAN (1 Tablet) (View Amoban Review and Amoban Label ), AZUCURENIN S (1.5 G) (View Azucurenin S Review and Azucurenin S Label ), NITOROL (3 Tablets) (View Nitorol Review and Nitorol Label ), COMELIAN (300 Mg) (View Comelian Review and Comelian Label ), TENAXIL (1 Mg) (View Tenaxil Review and Tenaxil Label ), DIACORT (90 Mg) (View Diacort Review and Diacort Label ).

5238598-6 | Blood Glucose Increased, Glycosylated Haemoglobin Increased, Renal Impairment
on Feb 05, 2007 Male patient from JAPAN , weighting 135.9 lb, was treated with Diart (View Usage). Patient experienced the following unwanted or unexpected effects: blood glucose increased, glycosylated haemoglobin increased, renal impairment. Diart dosage: 45 Mg. During the same period patient was treated with MEILAX (2 Tablets) (View Meilax Review and Meilax Label ), AMOBAN (1 Tablet) (View Amoban Review and Amoban Label ), AZUCURENIN S (1.5 G) (View Azucurenin S Review and Azucurenin S Label ), NITOROL (3 Tablets) (View Nitorol Review and Nitorol Label ), COMELIAN (300 Mg) (View Comelian Review and Comelian Label ), TENAXIL (1 Mg) (View Tenaxil Review and Tenaxil Label ), DIACORT (90 Mg) (View Diacort Review and Diacort Label ).


4949249-X | Brain Oedema, Depressed Level Of Consciousness, Disseminated Intravascular Coagulation, Epistaxis, Gaze Palsy, Grand Mal Convulsion, Haematemesis, Haematuria
on Jul 09, 2003 Female patient from JAPAN , 16 years of age, weighting 102.2 lb, was treated with Diart (View Usage). Patient had the following side effects: brain oedema, depressed level of consciousness, disseminated intravascular coagulation, epistaxis, gaze palsy, grand mal convulsion, haematemesis, haematuria. Diart dosage: 60 Mg/day. During the same period patient was treated with ALDACTONE (50 Mg/day) (View Aldactone Review and Aldactone Label ), ASPIRIN (100 Mgday) (View Aspirin Review and Aspirin Label ), ZANTAC (150 Mg/d) (View Zantac Review and Zantac Label ), EPADEL (1.8 G/d) (View Epadel Review and Epadel Label ), LASIX (240 Mg/d) (View Lasix Review and Lasix Label ), PREDNISOLONE (20 Mg/d) (View Prednisolone Review and Prednisolone Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ), WARFARIN (1 Mg/d) (View Warfarin Review and Warfarin Label ).


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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 Diart 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 Diart quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Diart 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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How Did You Deal with Side Effects?

During the same period patient was treated with DIART (1 Unit) (View Diart Review and Diart Label ), HUSCODE (View Huscode Review and Huscode Label ), FLOMOX ...

During the same period patient was treated with MAGMITT (Unk) (View Magmitt Review and Magmitt Label ), SELBEX (Unk) (View Selbex Review and Selbex Label ), DIART (Unk) (View ...

During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), ARTIST (View Artist Review and Artist Label ), DIART (View Diart Review ...

During the same period patient was treated with DIART (1 Unit) (View Diart Review and Diart Label ), HUSCODE (View Huscode Review and Huscode Label ), FLOMOX (View Flomox ...

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

... WARFARIN POTASSIUM (View Warfarin Potassium Review and Warfarin Potassium Label ), PEPCID (View Pepcid Review and Pepcid Label ), DIART (View Diart Review and Diart Label ), ...

... Bayaspirin (aspirin) Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), DIART (AZOSEMIDE) (View Diart (azosemide) Review and Diart ...

During the same period patient was treated with DIGOXIN, DIART, LASIX, RENIVACE, MEXITIL, ALDACTONE, SALOBEL, FAMOTIDINE. Patient was hospitalized.

During the same period patient was treated with MEXITIL (MXILETINE HYDROCHLORIDE), DIART (AZOSEMIDE), FLUITRAN (TRICHLORMETHIAZIDE), ASPIRIN, LANIRAPID (METILDIGOXIN), ...

During the same period patient was treated with ZYLORIC (200 Mg), FLUITRAN (2 Mg), TANKARU (3500 Mg), LASIX (80 Mg), DIART (40 Mg), ANPLAG (150 Mg), ALLEGRA (60 Mg).

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Diart Reactions
Blood Amylase Increased
Blood Glucose Increased
Brain Oedema
Depressed Level Of Consciousness
Disseminated Intravascular Coagulation
Epistaxis
Gaze Palsy
Glycosylated Haemoglobin Increased
Grand Mal Convulsion
Haematemesis
Haematuria
Renal Impairment
Diart 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 Diart 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!