CHRONIC FATIGUE SYNDROME side effect
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Drugs associated with CHRONIC FATIGUE SYNDROME
ACCUTANE ALEVE ALTACE AMBIEN BETASERON BEXTRA BYETTA DOPAMINE DURAGESIC ESCITALOPRAM FOSAMAX HYDROCORTONE IMMUNE LUNESTA PAXIL STEDIRIL XYREM ZELNORM ZOCORStediril Side Effects Report #5584772-9
Consumer or non-health professional from NETHERLANDS reported STEDIRIL problem on Dec 20, 2007. Female patient, 16 years of age, was diagnosed with abdominal pain and was treated with STEDIRIL. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, condition aggravated, . STEDIRIL dosage: unknown. During the same period patient was treated with PAROXETINE HYDROCHLORIDE, PANTOPRAZOLE, OXAZEPAM. Patient recovered.
Bextra Side Effects Report #5594947-0
BEXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2007. Female patient, 42 years of age, was diagnosed with chronic fatigue syndrome and was treated with BEXTRA. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, myocardial infarction, . BEXTRA dosage: 20 MG (20 MG,1 IN 1 D). Patient was hospitalized. Patient recovered.
Altace Side Effects Report #5525059-X
Consumer or non-health professional from UNITED KINGDOM reported ALTACE problem on Nov 12, 2007. Female patient was diagnosed with hypertension and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, pharyngolaryngeal pain, . ALTACE dosage: 2.5 MG, QD. During the same period patient was treated with NEBIVOLOL, LEVOTHYROXINE. Patient recovered.
Byetta Side Effects Report #5568028-6
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 05, 2007. Female patient, 59 years of age, weighting 254.9 lb, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, dyspepsia, energy increased, fibromyalgia, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, LUNESTA, AMLODIPINE BESYLATE, SINGULAIR, PULMICORT. Patient recovered.
Lunesta Side Effects Report #5492390-6
Consumer or non-health professional from UNITED STATES reported LUNESTA problem on July 17, 2007. Female patient, 38 years of age, weighting 115.0 lb, was diagnosed with insomnia and was treated with LUNESTA. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, poor quality sleep, somnolence, . LUNESTA dosage: 3 MG;HS;ORAL. During the same period patient was treated with ADVAIR DISKUS. Patient recovered.
Zelnorm Side Effects Report #5379752-2
ZELNORM problem was reported by a Physician from UNITED STATES on June 26, 2007. Female patient was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, fibromyalgia, lacunar infarction, loss of consciousness, . ZELNORM dosage: 6 MG, UNK. Patient recovered.
Zelnorm Side Effects Report #5379752-2
Physician from UNITED STATES reported ZELNORM problem on June 26, 2007. Female patient was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, fibromyalgia, lacunar infarction, loss of consciousness, . ZELNORM dosage: 6 MG, UNK. Patient recovered.
Zocor Side Effects Report #5759925-7
ZOCOR problem was reported by a Consumer or non-health professional from UNITED KINGDOM on May 30, 2008. Male patient, 59 years of age, was diagnosed with cerebrovascular accident prophylaxis, blood cholesterol increased, muscle twitching and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, . ZOCOR dosage: unknown. During the same period patient was treated with CLONAZEPAM. Patient was hospitalized. Patient recovered.
Dopamine Side Effects Report #5306431-X
Health Professional from UNITED KINGDOM reported DOPAMINE problem on Apr 10, 2007. Female patient, 50 years of age, weighting 112.4 lb, was diagnosed with periarthritis and was treated with DOPAMINE. After drug was administered, patient experienced the following problems/side effects: chronic fatigue syndrome, post viral fatigue syndrome, . DOPAMINE dosage: unknown. During the same period patient was treated with HYDROCORTISONE. Patient was hospitalized and became disabled. Patient recovered.
Aleve Side Effects Report #5658227-7
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 15, 2007. Female patient, 48 years of age, weighting 97.00 lb, was diagnosed with toothache, neuralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: asthenia, chronic fatigue syndrome, diarrhoea, dry mouth, dysstasia, gait disturbance, heart rate increased, loss of consciousness, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. During the same period patient was treated with IBUPROFEN, HYPERICUM, ELMIRON, LESSINA, ACT FLOURIDE RINSE, ESTER C, MINERALS. Patient recovered.
Escitalopram Side Effects Report #5692120-9
Consumer or non-health professional from DENMARK reported ESCITALOPRAM problem on Mar 14, 2008. Female patient, 27 years of age, was diagnosed with depression and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: anxiety, chronic fatigue syndrome, depression, hallucination, serotonin syndrome, social phobia, . ESCITALOPRAM dosage: 10 MG QD PO. During the same period patient was treated with IMOVANE, TRIPHASIL. Patient recovered.
Duragesic Side Effects Report #5771553-6
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on June 04, 2008. Female patient, weighting 175.0 lb, was diagnosed with sarcoidosis, gastrooesophageal reflux disease and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, chronic fatigue syndrome, feeling abnormal, fibromyalgia, hypertension, pain, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, NEXIUM, TYLENOL W. Patient was hospitalized. Patient recovered.
Xyrem Side Effects Report #5722745-3
Consumer or non-health professional from UNITED STATES reported XYREM problem on Apr 16, 2008. Female patient, 49 years of age, weighting 205.0 lb, was diagnosed with chronic fatigue syndrome, insomnia, convulsion and was treated with XYREM. After drug was administered, patient experienced the following problems/side effects: amnesia, chronic fatigue syndrome, convulsion, depression, dizziness, feeling abnormal, headache, ill-defined disorder, initial insomnia, . XYREM dosage: unknown. During the same period patient was treated with CLONAZEPAM, VALPROATE SEMI, PRAMIPEXOLE DIHYDROCHLORIDE, SOMATROPIN, PROGESTERONE, ESTRADIOL, TESTOSTERONE. Patient recovered.
Zelnorm Side Effects Report #5347270-3
ZELNORM problem was reported by a Physician from UNITED STATES on May 31, 2007. Female patient was diagnosed with irritable bowel syndrome and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, chronic fatigue syndrome, fibromyalgia, loss of consciousness, . ZELNORM dosage: 6 MG, UNK. Patient recovered.
Paxil Side Effects Report #5336884-2
Consumer or non-health professional from UNITED STATES reported PAXIL problem on May 24, 2007. Female patient, 30 years of age, weighting 170.0 lb, was diagnosed with death of relative and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: amnesia, chronic fatigue syndrome, confusional state, crying, depression, dizziness, epstein-barr virus infection, . PAXIL dosage: unknown. Patient recovered.
Zelnorm Side Effects Report #5308303-3
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 20, 2007. Female patient was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, chronic fatigue syndrome, fibromyalgia, loss of consciousness, . ZELNORM dosage: 6 MG, UNK. Patient recovered.
Zelnorm Side Effects Report #5308341-0
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on Apr 20, 2007. Female patient was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, chronic fatigue syndrome, fibromyalgia, loss of consciousness, . ZELNORM dosage: 6 MG, UNK. Patient recovered.
Fosamax Side Effects Report #5256886-4
FOSAMAX problem was reported by a Consumer or non-health professional from NEW ZEALAND on Feb 28, 2007. Female patient, 68 years of age, was diagnosed with osteoporosis, epilepsy and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: chest pain, chronic fatigue syndrome, dyspepsia, gastritis, hypertension, weight decreased, . FOSAMAX dosage: unknown. During the same period patient was treated with CARBAMAZEPINE. Patient was hospitalized. Patient recovered.
Ambien Side Effects Report #5268447-1
Consumer or non-health professional from UNITED KINGDOM reported AMBIEN problem on Mar 15, 2007. Male patient, weighting 187.4 lb, was treated with AMBIEN. After drug was administered, patient experienced the following problems/side effects: abnormal sleep-related event, chronic fatigue syndrome, feeling hot, injury, malaise, memory impairment, nervous system disorder, nuclear magnetic resonance imaging brain abnormal, pneumonia, . AMBIEN dosage: unknown. Patient recovered.
Immune Side Effects Report #5654146-0
IMMUNE GLOBULIN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2008. Female patient, 50 years of age, weighting 145.0 lb, was diagnosed with white blood cell count decreased and was treated with IMMUNE GLOBULIN. After drug was administered, patient experienced the following problems/side effects: abasia, asthenia, chronic fatigue syndrome, disease recurrence, dizziness, viral infection, . IMMUNE GLOBULIN dosage: 2 ML; Q6W; IM. During the same period patient was treated with ASPIRIN, XANAX. Patient recovered.
Accutane Side Effects Report #5724701-8
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on Apr 23, 2008. Female patient, weighting 143.1 lb, was diagnosed with oral contraception, musculoskeletal pain and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthritis, chronic fatigue syndrome, colitis, colitis ulcerative, dizziness, dry skin, eczema, gastritis, . ACCUTANE dosage: unknown. During the same period patient was treated with BIRTH CONTROL S, ORTHO TRI, ORTHO TRI, PHENERGAN, TYLENOL, ZANTAC, IBUPROFEN. Patient was hospitalized and became disabled. Patient recovered.
Betaseron Side Effects Report #5349954-X
BETASERON problem was reported by a Physician from GERMANY on May 24, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: antibody test positive, autoimmune thyroiditis, chronic fatigue syndrome, . BETASERON dosage: unknown. Patient recovered.
Hydrocortone Side Effects Report #5365893-2
Physician from UNITED KINGDOM reported HYDROCORTONE problem on June 08, 2007. Female patient, 34 years of age, was treated with HYDROCORTONE. After drug was administered, patient experienced the following problems/side effects: asthenia, binge eating, chronic fatigue syndrome, convulsion, dehydration, diabetes insipidus, disability, gait disturbance, gallbladder disorder, . HYDROCORTONE dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, DESMOPRESSIN. Patient recovered.
Accutane Side Effects Report #5318051-1
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 23, 2007. Male patient, 22 years of age, weighting 130.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, arthritis, chronic fatigue syndrome, crohn's disease, dizziness, gastrointestinal disorder, headache, inflammatory bowel disease, insomnia, . ACCUTANE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
Accutane Side Effects Report #5329757-2
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on May 08, 2007. Male patient, 22 years of age, weighting 130.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anaemia, arthritis, chronic fatigue syndrome, crohn's disease, diarrhoea, dizziness, emotional distress, gastrointestinal disorder, headache, . ACCUTANE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
Betaseron Side Effects Report #5333882-X
BETASERON problem was reported by a Physician from GERMANY on May 14, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: antibody test positive, autoimmune thyroiditis, chronic fatigue syndrome, hypothyroidism, . BETASERON dosage: unknown. Patient recovered.
Betaseron Side Effects Report #5307437-7
Physician from GERMANY reported BETASERON problem on Apr 10, 2007. Female patient, 30 years of age, weighting 116.8 lb, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: antibody test positive, autoimmune thyroiditis, chronic fatigue syndrome, hypothyroidism, . BETASERON dosage: unknown. Patient recovered.