VITAMIN D DECREASED side effect
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Drugs associated with VITAMIN D DECREASED
ACTOS ADVAIR BYETTA CRESTOR FORTEO HUMIRA LIPITOR RECLAST TRILEPTAL VYTORINCrestor Side Effects Report #5563416-6
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on Apr 23, 2007. Female patient, 68 years of age, weighting 151.9 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: vitamin d decreased, . CRESTOR dosage: unknown. During the same period patient was treated with CALTRATE PLUS D. Patient recovered.
Lipitor Side Effects Report #5551429-X
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 18, 2007. Female patient, 75 years of age, weighting 125.0 lb, was diagnosed with prophylaxis and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: vitamin d decreased, . LIPITOR dosage: 10 MG (10 MG, 1 IN 1 D). During the same period patient was treated with PLAVIX, VITAMIN, VITAMIN C, FOLIC ACID, FOSAMAX, OMEGA. Patient recovered.
Forteo Side Effects Report #5584457-9
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Dec 31, 2007. Female patient, 59 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: pelvic fracture, vitamin d decreased, . FORTEO dosage: unknown. Patient recovered.
Forteo Side Effects Report #5575223-9
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 18, 2007. Female patient, 59 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: pubic rami fracture, vitamin d decreased, . FORTEO dosage: unknown. Patient recovered.
Vytorin Side Effects Report #5447253-9
Consumer or non-health professional from UNITED STATES reported VYTORIN problem on Sept 05, 2007. Male patient, weighting 186.7 lb, was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: pain, vitamin d decreased, . VYTORIN dosage: unknown. Patient recovered.
Vytorin Side Effects Report #5456404-1
VYTORIN problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 17, 2007. Male patient, weighting 186.7 lb, was diagnosed with unevaluable event and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: pain, vitamin d decreased, . VYTORIN dosage: unknown. Patient recovered.
Reclast Side Effects Report #5739778-3
Consumer or non-health professional from UNITED STATES reported RECLAST problem on May 12, 2008. Female patient, 56 years of age, weighting 117.0 lb, was diagnosed with resorption bone increased and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: pain in extremity, vitamin d decreased, . RECLAST dosage: unknown. Patient recovered.
Byetta Side Effects Report #5575140-4
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 11, 2007. Female patient, 61 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, decreased appetite, vitamin d decreased, . BYETTA dosage: unknown. Patient recovered.
Advair Side Effects Report #5496233-6
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on May 22, 2007. Female patient, 48 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: cough, vitamin d decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with LASIX, SINGULAIR, ZYRTEC. Patient recovered.
Actos Side Effects Report #5501647-1
ACTOS problem was reported by a Consumer or non-health professional from FRANCE on Oct 15, 2007. Female patient, 58 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: fall, femoral neck fracture, vitamin d decreased, . ACTOS dosage: (30 MG, 1 D) ORAL. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5771125-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on May 29, 2008. Female patient, weighting 150.1 lb, was diagnosed with rheumatoid arthritis, gastrooesophageal reflux disease, blood pressure, vitamin d decreased and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: accidental exposure, injection site irritation, vitamin d decreased, . HUMIRA dosage: unknown. During the same period patient was treated with ESTROGENS CONJUGATED, ESOMEPRAZOLE MAGNESIUM, THYROID LEVOXYL, VALSARTAN, DYAZIDE, ERGOCALCIFEROL. Patient recovered.
Trileptal Side Effects Report #5675535-4
TRILEPTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 29, 2007. Female patient was diagnosed with fibromyalgia and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: confusional state, disturbance in attention, vitamin d decreased, . TRILEPTAL dosage: 150 MG QAM, 300 MG QHS, ORAL. Patient recovered.