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Ergocalciferol adverse events reported to FDA.

Have You Experienced unusual Ergocalciferol symptoms? PatientsVille.com collects and analyzes Ergocalciferol side effect and adverse reports submitted by Ergocalciferol users, such as .

Summary

FDA Adverse Reports: 11. View All

Ergocalciferol FDA safety alerts: No

Reported hospitalizations: 3

Ergocalciferol Dosage, Warnings, Usage.

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

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7005205-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Atrial Fibrillation, Blood Creatinine Increased, Hypervitaminosis D
on Sep 20, 2010 Male patient from UNITED STATES , 61 years of age, weighting 220.0 lb, was diagnosed with vitamin d, vitamin supplementation and was treated with Ergocalciferol (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, atrial fibrillation (What is atrial fibrillation?), blood creatinine increased, hypervitaminosis d. Ergocalciferol dosage: 50000 Iu Qweek Po. Patient was hospitalized.

6915323-1 | Hypersensitivity
Patient was taking Ergocalciferol (View Usage). Patient had the following side effects: hypersensitivity on Aug 06, 2010 from UNITED STATES Additional patient health information: Female patient , 34 years of age, weighting 138.0 lb, was diagnosed with vitamin d decreased and. Ergocalciferol dosage: 50,000 Iu Once A Week Po.

6678248-5 | Blister
Adverse event was reported on Apr 08, 2010 by a Male patient taking Ergocalciferol (View Usage) (Dosage: 50000 Qweek Po) was diagnosed with vitamin d decreased and. Location: UNITED STATES , 53 years of age, weighting 214.5 lb, After Ergocalciferol was administered, patient had the following side effects: blister.

6649996-8 | Bone Disorder, Bone Pain
on Mar 24, 2010 Female patient from UNITED STATES , 70 years of age, weighting 170.0 lb, was diagnosed with vitamin d deficiency and was treated with Ergocalciferol (View Usage). Patient experienced the following unwanted or unexpected effects: bone disorder, bone pain. Ergocalciferol dosage: 1 For 8 Weeks Per Week Oral : 1 For 12 Months Per Month Didn't Take.


6526715-7 | Asthenia, Breast Swelling, Dizziness, Incorrect Dose Administered, Myalgia, Oedema Peripheral
on Jan 04, 2010 Female patient from UNITED STATES , 67 years of age, weighting 220.0 lb, was diagnosed with vitamin d deficiency and was treated with Ergocalciferol (View Usage). Patient had the following side effects: asthenia, breast swelling, dizziness (What is dizziness?), incorrect dose administered, myalgia, oedema peripheral. Ergocalciferol dosage: 50,000 Unit Cap 1 Pill/week Swallow.

6504566-7 | Anaphylactic Shock
Patient was taking Ergocalciferol (View Usage). After Ergocalciferol was administered, patient had the following side effects: anaphylactic shock on Dec 11, 2009 from UNITED STATES Additional patient health information: Female patient , 71 years of age, was diagnosed with vitamin d deficiency and. Ergocalciferol dosage: Oral Prior To 11/26/09. Patient was hospitalized.

6356598-X | Asthenia, Migraine, Muscle Injury, Nerve Injury, Sinus Disorder, Sleep Disorder, Unevaluable Event, Weight Decreased
Adverse event was reported on Sep 10, 2009 by a Female patient taking Ergocalciferol (View Usage) (Dosage: 1 Capsule Every Week Po) was diagnosed with osteoporosis (What is osteoporosis?) and. Location: UNITED STATES , 74 years of age, weighting 116.0 lb, Patient experienced the following unwanted or unexpected effects: asthenia, migraine (What is migraine?), muscle injury, nerve injury, sinus disorder, sleep disorder (What is sleep disorder?), unevaluable event, weight decreased. Patient was hospitalized.

5793061-9 | Angiotensin Converting Enzyme Increased, Blood 1,25-dihydroxycholecalciferol Increased, Blood Creatinine Increased, Blood Urea Increased, Constipation, Hypercalcaemia, Lethargy, No Therapeutic Response
on Jun 09, 2008 Male patient from UNITED STATES , 66 years of age, was treated with Ergocalciferol (View Usage). Patient had the following side effects: angiotensin converting enzyme increased, blood 1,25-dihydroxycholecalciferol increased, blood creatinine increased, blood urea increased, constipation (What is constipation?), hypercalcaemia, lethargy, no therapeutic response. Ergocalciferol dosage: 50000 Iu/m.

5787660-8 | Dysstasia, Gait Disturbance, Muscular Weakness
on Jun 23, 2008 Female patient from UNITED STATES , 79 years of age, weighting 136.0 lb, was diagnosed with vitamin d decreased and was treated with Ergocalciferol (View Usage). After Ergocalciferol was administered, patient had the following side effects: dysstasia, gait disturbance, muscular weakness. Ergocalciferol dosage: One Once A Week One Time Only.

5452043-7 | Back Pain, Flank Pain, Nephrolithiasis
Patient was taking Ergocalciferol (View Usage). Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), flank pain, nephrolithiasis on Jul 16, 2007 from UNITED STATES Additional patient health information: Female patient , 61 years of age, was diagnosed with osteoporosis (What is osteoporosis?) and. Ergocalciferol dosage: 1 Capsule Weekly, Oral; Then 1 Capsule Qow. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), ORAL CONTRACEPTIVES (View Oral Contraceptives Review and Oral Contraceptives Label ), HEPARIN (View Heparin Review and Heparin Label ), KENALOG PERANTIL (View Kenalog Perantil Review and Kenalog Perantil Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

5355334-3 | Blood Calcium Abnormal, Chapped Lips, Dizziness, Dry Mouth, Gastrointestinal Pain, Granulomatous Liver Disease, Haematochezia, Headache, Muscular Weakness
Adverse event was reported on Jun 04, 2007 by a Female patient taking Ergocalciferol (View Usage) (Dosage: 2 Capsules/weekly) was diagnosed with hypoparathyroidism and. Location: UNITED STATES , 52 years of age, Patient had the following side effects: blood calcium abnormal, chapped lips, dizziness (What is dizziness?), dry mouth, gastrointestinal pain, granulomatous liver disease, haematochezia, headache (What is headache?), muscular weakness. During the same period patient was treated with BENTYL (View Bentyl Review and Bentyl Label ), BUSPAR (View Buspar Review and Buspar Label ), PREVACID (View Prevacid Review and Prevacid Label ), SINGULAIR (View Singulair Review and Singulair Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), XANAX (View Xanax Review and Xanax Label ), ACETAMINOPHEN W/ CODEINE (View Acetaminophen W/ Codeine Review and Acetaminophen W/ Codeine Label ), ... (View ... Review and ... Label ).


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Ergocalciferol Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

CAROL   cOLORADO 

12:42pm on Friday, November 26th, 2010

What are the POSITIVE positive effects of ergocalciferol treatment? Does anyone actually feel BETTER... read more »

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 Ergocalciferol 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 Ergocalciferol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ergocalciferol 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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Rheumatoid arthritis (RA) is a form of arthritis that

During the same period patient was treated with MULTIVITAMINS (ASCORBIC ACID, ERGOCALCIFEROL, FOLIC ACID, NICOTINAMIDE (View Multivitamins (ascorbic Acid ...

During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ), RETINOL (View Retinol Review and Retinol Label ), ERGOCALCIFEROL (View ...

During the same period patient was treated with CALCIUM+D (View Calcium+d Review and Calcium+d Label ), ERGOCALCIFEROL (View Ergocalciferol Review and Ergocalciferol Label ...

During the same period patient was treated with MULTIVITAMINS (ASCORBIC ACID, ERGOCALCIFEROL, FOLIC ACID, NICOTINAMIDE (View Multivitamins (ascorbic Acid, Ergocalciferol ...

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

... paracetamol, Oxycodone Hydrochloride) Review and Percocet /00867901/ (paracetamol, Oxycodone Hydrochloride) Label ), MULTIVITAMINS (ASCORBIC ACID, ERGOCALCIFEROL, FOLIC ...

ergocalciferol Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: erlotinib Episodes: 1: Diagnosed with major depression ...

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Ergocalciferol Reactions
Alanine Aminotransferase Increased
Anaphylactic Shock
Angiotensin Converting Enzyme Increased
Aspartate Aminotransferase Increased
Asthenia
Atrial FibrillationWhat is Atrial fibrillation?
Back PainWhat is Back pain?
Blister
Blood 1,25-dihydroxycholecalciferol Increased
Blood Calcium Abnormal
Blood Creatinine Increased
Blood Urea Increased
Bone Disorder
Bone Pain
Breast Swelling
Chapped Lips
ConstipationWhat is Constipation?
DizzinessWhat is Dizziness?
Dry Mouth
Dysstasia
Flank Pain
Gait Disturbance
Gastrointestinal Pain
Granulomatous Liver Disease
Haematochezia
HeadacheWhat is Headache?
Hypercalcaemia
Hypersensitivity
Hypervitaminosis D
Muscular Weakness
Ergocalciferol 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 Ergocalciferol 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!