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Citalor adverse events reported to FDA.

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Summary

FDA Adverse Reports: 14. View All

Citalor FDA safety alerts: No

Reported deaths: 8

Reported hospitalizations: 22

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

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6900560-2 | Dizziness, Presyncope, Prostatic Disorder
on Jul 26, 2010 Male patient from BRAZIL , 59 years of age, weighting 198.4 lb, was diagnosed with blood cholesterol increased and was treated with Citalor (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), presyncope, prostatic disorder. Citalor dosage: 20 Mg, 1x/day. During the same period patient was treated with ASPIRIN (100 Mg, 1x/day) (View Aspirin Review and Aspirin Label ).

6887476-5 | Neuritis, Tendonitis
Patient was taking Citalor (View Usage). Patient had the following side effects: neuritis, tendonitis on Jul 21, 2010 from BRAZIL Additional patient health information: Female patient , 67 years of age, . Citalor dosage: Unk. During the same period patient was treated with XALATAN (Unk) (View Xalatan Review and Xalatan Label ), COSOPT (Unk) (View Cosopt Review and Cosopt Label ), IRBESARTAN (View Irbesartan Review and Irbesartan Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

6875343-2 | Dizziness, Presyncope, Prostatic Disorder
Adverse event was reported on Jul 16, 2010 by a Male patient taking Citalor (View Usage) (Dosage: 20 Mg, 1x/day) was diagnosed with blood cholesterol and. Location: BRAZIL , 59 years of age, weighting 198.4 lb, After Citalor was administered, patient had the following side effects: dizziness (What is dizziness?), presyncope, prostatic disorder.

6856529-X | Blood Cholesterol Increased, Constipation, Flatulence, Oesophagitis, Tinnitus
on Jul 12, 2010 Female patient from BRAZIL , 56 years of age, weighting 127.9 lb, was diagnosed with blood cholesterol increased and was treated with Citalor (View Usage). Patient experienced the following unwanted or unexpected effects: blood cholesterol increased, constipation (What is constipation?), flatulence, oesophagitis, tinnitus (What is tinnitus?). Citalor dosage: 10 Mg, Unk. During the same period patient was treated with OLCADIL (1 Mg, Unk) (View Olcadil Review and Olcadil Label ).


6724550-8 | Blood Pressure Fluctuation, Dizziness, Neck Pain
on May 06, 2010 Female patient from BRAZIL , 84 years of age, was diagnosed with hypercholesterolaemia, hypertension, thrombosis prophylaxis and was treated with Citalor (View Usage). Patient had the following side effects: blood pressure fluctuation, dizziness (What is dizziness?), neck pain. Citalor dosage: 10 Mg, Three Times Weekly. During the same period patient was treated with NORVASC (2.5 Mg (half Of 5 Mg Tablet), 1x/day) (View Norvasc Review and Norvasc Label ), PROPRANOLOL (Unk) (View Propranolol Review and Propranolol Label ), SUSTRATE (Unk) (View Sustrate Review and Sustrate Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ).

6707560-6 | Blood Cholesterol Increased, Constipation, Flatulence, Oesophagitis
Patient was taking Citalor (View Usage). After Citalor was administered, patient had the following side effects: blood cholesterol increased, constipation (What is constipation?), flatulence, oesophagitis on Apr 23, 2010 from BRAZIL Additional patient health information: Female patient , 56 years of age, weighting 127.9 lb, was diagnosed with blood cholesterol increased and. Citalor dosage: 10 Mg, Unk. During the same period patient was treated with OLCADIL (1 Mg, Unk) (View Olcadil Review and Olcadil Label ).

6454271-0 | Breast Mass, Nipple Pain
Adverse event was reported on Nov 16, 2009 by a Male patient taking Citalor (View Usage) (Dosage: 20 Mg, 1x/day) was diagnosed with hypercholesterolaemia and. Location: BRAZIL , 29 years of age, weighting 194.0 lb, Patient experienced the following unwanted or unexpected effects: breast mass, nipple pain.

6448547-0 | Gastrointestinal Carcinoma
on Nov 10, 2009 Female patient from BRAZIL , 57 years of age, weighting 176.4 lb, was diagnosed with angina pectoris, blood cholesterol and was treated with Citalor (View Usage). Patient had the following side effects: gastrointestinal carcinoma. Citalor dosage: 10 Mg, 1x/day. During the same period patient was treated with DILACORON (Unk) (View Dilacoron Review and Dilacoron Label ), SUSTRATE (Unk) (View Sustrate Review and Sustrate Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), A.A.S. (Unk) (View A.a.s. Review and A.a.s. Label ).

6437842-7 | Abdominal Discomfort, Apnoea, Blood Cholesterol Increased, Diabetes Mellitus, Fluid Retention, Hypoaesthesia, Limb Injury, Malaise
on Nov 03, 2009 Female patient from BRAZIL , 51 years of age, weighting 216.1 lb, was diagnosed with hypercholesterolaemia and was treated with Citalor (View Usage). After Citalor was administered, patient had the following side effects: abdominal discomfort, apnoea, blood cholesterol increased, diabetes mellitus, fluid retention, hypoaesthesia, limb injury, malaise. Citalor dosage: 20 Mg, 1x/day. During the same period patient was treated with SIMVASTATIN (20 Mg, Unk) (View Simvastatin Review and Simvastatin Label ), ATACAND (Unk) (View Atacand Review and Atacand Label ), ATENOLOL (Unk) (View Atenolol Review and Atenolol Label ), SOMALGIN (Unk) (View Somalgin Review and Somalgin Label ), PLASIL (Unk) (View Plasil Review and Plasil Label ).

5928344-2 | Anxiety, Diabetes Mellitus, Headache, Heart Rate Increased, Heart Rate Irregular, High Density Lipoprotein Decreased, Insomnia
Patient was taking Citalor (View Usage). Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), diabetes mellitus, headache (What is headache?), heart rate increased, heart rate irregular, high density lipoprotein decreased, insomnia on Oct 15, 2008 from BRAZIL Additional patient health information: Female patient , weighting 147.7 lb, was diagnosed with blood cholesterol increased and. Citalor dosage: . During the same period patient was treated with SANDRENA (View Sandrena Review and Sandrena Label ), EUTHYROX (View Euthyrox Review and Euthyrox Label ), CLORANA (View Clorana Review and Clorana Label ), LOSARTAN (View Losartan Review and Losartan Label ).

5877190-7 | Blood Cholesterol Increased, Blood Creatine Phosphokinase Increased, Myalgia
Adverse event was reported on Sep 01, 2008 by a Female patient taking Citalor (View Usage) (Dosage: ) was diagnosed with blood cholesterol increased, hypothyroidism, hypertension and. Location: BRAZIL , weighting 178.6 lb, Patient had the following side effects: blood cholesterol increased, blood creatine phosphokinase increased, myalgia. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ).

5818253-1 | Arterial Occlusive Disease, Blood Cholesterol Decreased, Blood Testosterone Abnormal, Chest Pain, Libido Decreased, Obesity Surgery, Pain In Extremity
on Jul 11, 2008 Male patient from BRAZIL , weighting 180.8 lb, was diagnosed with blood cholesterol increased, arteriosclerosis and was treated with Citalor (View Usage). After Citalor was administered, patient had the following side effects: arterial occlusive disease, blood cholesterol decreased, blood testosterone abnormal, chest pain (What is chest pain?), libido decreased, obesity surgery, pain in extremity. Citalor dosage: . During the same period patient was treated with AAS (View Aas Review and Aas Label ), SELOZOK (View Selozok Review and Selozok Label ). Patient was hospitalized.

5799416-0 | Catheterisation Cardiac
on Jun 25, 2008 Male patient from BRAZIL , weighting 187.4 lb, was diagnosed with blood cholesterol increased and was treated with Citalor (View Usage). Patient experienced the following unwanted or unexpected effects: catheterisation cardiac. Citalor dosage: . During the same period patient was treated with SELOZOK (View Selozok Review and Selozok Label ), AAS (View Aas Review and Aas Label ).

5799384-1 | Blood Cholesterol Decreased, Blood Testosterone Abnormal, Libido Decreased, Obesity Surgery
Patient was taking Citalor (View Usage). Patient had the following side effects: blood cholesterol decreased, blood testosterone abnormal, libido decreased, obesity surgery on Jun 25, 2008 from BRAZIL Additional patient health information: Male patient , weighting 187.4 lb, was diagnosed with blood cholesterol increased and. Citalor dosage: . During the same period patient was treated with AAS (View Aas Review and Aas Label ), SELOZOK (View Selozok Review and Selozok 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 Citalor 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 Citalor quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Citalor 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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Citalor Reactions
Abdominal Discomfort
AnxietyWhat is Anxiety?
Apnoea
Arterial Occlusive Disease
Blood Cholesterol Decreased
Blood Cholesterol Increased
Blood Creatine Phosphokinase Increased
Blood Pressure Fluctuation
Blood Testosterone Abnormal
Breast Mass
Catheterisation Cardiac
Chest PainWhat is Chest pain?
ConstipationWhat is Constipation?
Diabetes Mellitus
DizzinessWhat is Dizziness?
Flatulence
Fluid Retention
Gastrointestinal Carcinoma
HeadacheWhat is Headache?
Heart Rate Increased
Heart Rate Irregular
High Density Lipoprotein Decreased
Hypoaesthesia
Insomnia
Libido Decreased
Limb Injury
Obesity Surgery
Oesophagitis
Presyncope
Prostatic Disorder
Citalor 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 Citalor 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!