DECREASED ACTIVITY side effect
What is DECREASED ACTIVITY ?Drugs associated with DECREASED ACTIVITY
ACTOS ALPRAZOLAM AOTAL AVANDIA AVELOX BEXTRA BYETTA CELEBREX CHAMPIX CHANTIX COREG CYMBALTA DILANTIN DULOXETINE EFFEXOR ENBREL EPITOMAX FAZACLO FLUOXETINE FORTEO GENOTROPIN HUMIRA LIPITOR LOVASTATIN LUVOX MAGNEVIST METOPROLOL MYOZYME NEXIUM NITRIC PIMOZIDE PROCRIT REVATIO RIFABUTIN RISPERDAL ROSIGLITAZONE ROZEREM SEVREDOL SIMVASTATIN SINGULAIR SOLANAX TEKTURNA TEMODAL TOFRANIL TOPAMAX TRACLEER TYKERB VALIUM VELCADE VYVANSE ZELMAC ZYPREXA ZYRTECDECREASED ACTIVITY : Singulair Side Effects Report #5690629-5
Consumer or non-health professional from UNITED STATES reported SINGULAIR problem on Mar 31, 2008. Male patient, 53 years of age, weighting 290.0 lb, was diagnosed with hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: decreased activity, depression, hypersomnia, lethargy, . SINGULAIR dosage: 5 MG -? HALF DOSE- DAILY PO. Patient recovered.
DECREASED ACTIVITY : Tracleer Side Effects Report #5632706-0
TRACLEER problem was reported by a Physician from UNITED STATES on Feb 01, 2008. Male patient, 81 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: decreased activity, dysuria, feeling abnormal, malaise, oedema peripheral, pulmonary embolism, thrombosis, urinary retention, urine flow decreased, . TRACLEER dosage: 62.5 MG, BID, ORAL. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Sevredol Side Effects Report #5581593-8
Pharmacist from SPAIN reported SEVREDOL problem on Dec 28, 2007. Male patient, 76 years of age, was diagnosed with post herpetic neuralgia and was treated with SEVREDOL. After drug was administered, patient experienced the following problems/side effects: decreased activity, dyspnoea, somnolence, . SEVREDOL dosage: 10 MG, 12 TABLETS. During the same period patient was treated with SPIRIVA, SERETIDE, ACETYLCYSTEINE, CIPROFLOXACIN. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Enbrel Side Effects Report #5546880-8
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: decreased activity, infection, malaise, middle ear effusion, rosacea, weight increased, . ENBREL dosage: unknown. During the same period patient was treated with METHOTREXATE, CELEBREX, FOLIC ACID, PREVACID, TOPROL, HYDROCHLOROTHIAZIDE, ATENOLOL, RHINOCORT. Patient recovered.
DECREASED ACTIVITY : Actos Side Effects Report #5572315-5
Consumer or non-health professional from GERMANY reported ACTOS problem on Dec 10, 2007. Female patient, 79 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: decreased activity, humerus fracture, hyperglycaemia, pain, . ACTOS dosage: 30 MG (30 MG, 1 - 0 - 0 TABLET PER ORAL. During the same period patient was treated with METFORMIN, ACETYLSALICYLIC ACID SRT, RAMIPRIL, METOPROLOL SUCCINATE, SIMVA. Patient was hospitalized and became disabled. Patient recovered.
DECREASED ACTIVITY : Bextra Side Effects Report #5596304-X
BEXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 16, 2007. Female patient, 69 years of age, was diagnosed with nerve injury, pain and was treated with BEXTRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, depression, gastrointestinal disorder, nausea, obesity, . BEXTRA dosage: unknown. During the same period patient was treated with CELEBREX, DARVOCET, CHLORTHALIDONE, PAXIL. Patient recovered.
DECREASED ACTIVITY : Duloxetine Side Effects Report #5509961-0
Physician from UNITED STATES reported DULOXETINE problem on Nov 07, 2007. Female patient, 65 years of age, weighting 200.0 lb, was diagnosed with major depression, pain and was treated with DULOXETINE. After drug was administered, patient experienced the following problems/side effects: decreased activity, disturbance in attention, dyspnoea exertional, hypertension, impaired work ability, malaise, tachycardia, wheezing, . DULOXETINE dosage: 10-60MG DAILY PO. During the same period patient was treated with LISINOPRIL, AMLODIPINE, HYDROCHLOROTHIAZIDE, PROPRANOLOL, METOPROLOL TARTRATE, HYDRALAZINE. Patient recovered.
DECREASED ACTIVITY : Risperdal Side Effects Report #5513125-4
RISPERDAL problem was reported by a Physician from GERMANY on Nov 06, 2007. Female patient, weighting 132.3 lb, was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: decreased activity, hypotension, intentional overdose, suicide attempt, tachycardia, . RISPERDAL dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Coreg Side Effects Report #5515640-6
Consumer or non-health professional from UNITED STATES reported COREG problem on July 19, 2007. Female patient, 79 years of age, was diagnosed with hypertension and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: decreased activity, feeling abnormal, sluggishness, . COREG dosage: unknown. During the same period patient was treated with PAROXETINE, PAXIL. Patient recovered.
DECREASED ACTIVITY : Forteo Side Effects Report #5522220-5
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 06, 2007. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: decreased activity, fall, injection site haemorrhage, lower limb fracture, muscular weakness, pelvic fracture, resorption bone increased, upper limb fracture, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Chantix Side Effects Report #5525837-7
Physician from UNITED STATES reported CHANTIX problem on Nov 14, 2007. Female patient, weighting 89.95 lb, was diagnosed with tobacco abuse and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: decreased activity, depressed mood, treatment noncompliance, . CHANTIX dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Rozerem Side Effects Report #5529029-7
ROZEREM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2007. Male patient, 57 years of age, weighting 237.0 lb, was diagnosed with insomnia, middle insomnia and was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: decreased activity, hangover, middle insomnia, . ROZEREM dosage: 8 MG, QHS, PER ORAL. Patient recovered.
DECREASED ACTIVITY : Pimozide Side Effects Report #5530408-2
Consumer or non-health professional from GERMANY reported PIMOZIDE problem on Nov 15, 2007. Male patient, 21 years of age, was treated with PIMOZIDE. After drug was administered, patient experienced the following problems/side effects: decreased activity, suicide attempt, . PIMOZIDE dosage: unknown. During the same period patient was treated with TIAPRIDE HYDROCHLORIDE, ZOPICLONE. Patient recovered.
DECREASED ACTIVITY : Byetta Side Effects Report #5577728-3
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on June 22, 2007. Male patient, 65 years of age, was diagnosed with insulin resistant diabetes and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: decreased activity, decreased appetite, feeling abnormal, headache, . BYETTA dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Luvox Side Effects Report #5489571-4
Pharmacist from UNITED STATES reported LUVOX problem on Oct 16, 2007. Female patient, 60 years of age, weighting 198.4 lb, was treated with LUVOX. After drug was administered, patient experienced the following problems/side effects: decreased activity, incontinence, serotonin syndrome, . LUVOX dosage: 200 MG BID PO. During the same period patient was treated with TOPAMAX. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Chantix Side Effects Report #5494052-8
CHANTIX problem was reported by a Physician from UNITED STATES on Oct 11, 2007. Female patient was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: decreased activity, depressed mood, . CHANTIX dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Myozyme Side Effects Report #5502311-5
Health Professional from UNITED STATES reported MYOZYME problem on Oct 15, 2007. Male patient, 42 years of age, weighting 152.1 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: decreased activity, disease progression, glycogen storage disease type ii, vital capacity decreased, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with TENORMIN, PLENDIL. Patient recovered.
DECREASED ACTIVITY : Champix Side Effects Report #5453122-0
CHAMPIX problem was reported by a Health Professional from UNITED KINGDOM on Sept 04, 2007. Female patient, 32 years of age, weighting 140.0 lb, was diagnosed with contraception and was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: decreased activity, impaired work ability, nausea, vomiting, . CHAMPIX dosage: unknown. During the same period patient was treated with LOESTRIN. Patient recovered.
DECREASED ACTIVITY : Humira Side Effects Report #5453167-0
Consumer or non-health professional from CANADA reported HUMIRA problem on Sept 04, 2007. Male patient, weighting 170.2 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, sepsis, . HUMIRA dosage: unknown. Patient died on 08/21/2007.
DECREASED ACTIVITY : Avelox Side Effects Report #5462960-X
AVELOX problem was reported by a Consumer or non-health professional from BELGIUM on Sept 17, 2007. Male patient, 41 years of age, was diagnosed with bronchitis and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: decreased activity, . AVELOX dosage: UNIT DOSE: 400 MG. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Forteo Side Effects Report #5404048-X
Consumer or non-health professional from UNITED STATES reported FORTEO problem on July 23, 2007. Female patient, 86 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: decreased activity, fall, injection site haemorrhage, muscular weakness, pelvic fracture, upper limb fracture, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Cymbalta Side Effects Report #5407471-2
CYMBALTA problem was reported by a Physician from UNITED STATES on July 25, 2007. Female patient, 85 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: decreased activity, drooling, flat affect, lack of spontaneous speech, tardive dyskinesia, . CYMBALTA dosage: 60 MG, UNK. During the same period patient was treated with ARICEPT, NAMENDA, PLAVIX, XANAX, FOLIC ACID, TOPROL. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Humira Side Effects Report #5431587-8
Consumer or non-health professional from CANADA reported HUMIRA problem on Aug 24, 2007. Male patient, weighting 170.2 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, pneumonia, . HUMIRA dosage: unknown. Patient died on 08/21/2007.
DECREASED ACTIVITY : Humira Side Effects Report #5437390-7
HUMIRA problem was reported by a Consumer or non-health professional from CANADA on Aug 24, 2007. Male patient, weighting 170.2 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, mobility decreased, pneumonia, . HUMIRA dosage: unknown. Patient died on 08/21/2007.
DECREASED ACTIVITY : Zyprexa Side Effects Report #5387459-0
Physician from JAPAN reported ZYPREXA problem on July 02, 2007. Female patient, 51 years of age, weighting 179.1 lb, was diagnosed with schizophrenia and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: decreased activity, increased appetite, metabolic syndrome, weight increased, . ZYPREXA dosage: unknown. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Procrit Side Effects Report #5398360-0
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Male patient, weighting 165.1 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: decreased activity, fatigue, feeling abnormal, . PROCRIT dosage: unknown. During the same period patient was treated with ZOCOR. Patient recovered.
DECREASED ACTIVITY : Zyprexa Side Effects Report #5387459-0
Physician from JAPAN reported ZYPREXA problem on July 02, 2007. Female patient, 51 years of age, weighting 179.1 lb, was diagnosed with schizophrenia and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: decreased activity, increased appetite, metabolic syndrome, weight increased, . ZYPREXA dosage: unknown. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Procrit Side Effects Report #5398360-0
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Male patient, weighting 165.1 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: decreased activity, fatigue, feeling abnormal, . PROCRIT dosage: unknown. During the same period patient was treated with ZOCOR. Patient recovered.
DECREASED ACTIVITY : Velcade Side Effects Report #5656254-7
Physician from JAPAN reported VELCADE problem on Feb 21, 2008. Male patient was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: anorexia, decreased activity, malaise, pancytopenia, sepsis, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. Patient recovered.
DECREASED ACTIVITY : Chantix Side Effects Report #5662199-9
CHANTIX problem was reported by a Health Professional from UNITED KINGDOM on Mar 04, 2008. Female patient, 59 years of age, weighting 140.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: aggression, decreased activity, insomnia, panic attack, paranoia, somnolence, . CHANTIX dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Revatio Side Effects Report #5676386-7
Consumer or non-health professional from UNITED STATES reported REVATIO problem on Mar 11, 2008. Male patient, weighting 185.0 lb, was diagnosed with pulmonary hypertension and was treated with REVATIO. After drug was administered, patient experienced the following problems/side effects: cough, decreased activity, pain in extremity, paraesthesia, sinus headache, . REVATIO dosage: unknown. During the same period patient was treated with WARFARIN, NONSELECTIVE ENDOTHELIN RECEPTOR ANTAGONIST. Patient recovered.
DECREASED ACTIVITY : Avelox Side Effects Report #5690612-X
AVELOX problem was reported by a Health Professional from UNITED STATES on Mar 31, 2008. Female patient, 51 years of age, weighting 135.0 lb, was diagnosed with sinusitis and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: arthralgia, decreased activity, gait disturbance, joint swelling, pain in extremity, . AVELOX dosage: 400MG 1 TIME / DAY PO. Patient recovered.
DECREASED ACTIVITY : Magnevist Side Effects Report #5633064-8
Consumer or non-health professional from UNITED STATES reported MAGNEVIST problem on Feb 11, 2008. Female patient was diagnosed with nuclear magnetic resonance imaging and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: anxiety, decreased activity, emotional distress, fibrosis, injury, joint contracture, nephrogenic systemic fibrosis, pain, . MAGNEVIST dosage: unknown. During the same period patient was treated with OMNISCAN. Patient recovered.
DECREASED ACTIVITY : Effexor Side Effects Report #5564743-9
EFFEXOR problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 13, 2007. Female patient, 58 years of age, weighting 135.0 lb, was diagnosed with depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: arthralgia, decreased activity, pain in extremity, . EFFEXOR dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Avandia Side Effects Report #5571761-3
Physician from FRANCE reported AVANDIA problem on Dec 18, 2007. Female patient, weighting 262.4 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: cardiac failure, decreased activity, dyspnoea exertional, fluid retention, weight increased, . AVANDIA dosage: 4MG PER DAY. During the same period patient was treated with TRIAMCINOLONE. Patient recovered.
DECREASED ACTIVITY : Avandia Side Effects Report #5576524-0
AVANDIA problem was reported by a Physician from FRANCE on Dec 18, 2007. Female patient, weighting 262.4 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: cardiac failure, decreased activity, dyspnoea exertional, fluid retention, weight increased, . AVANDIA dosage: 4MG PER DAY. During the same period patient was treated with TRIAMCINOLONE. Patient recovered.
DECREASED ACTIVITY : Avelox Side Effects Report #5579096-X
Consumer or non-health professional from UNITED STATES reported AVELOX problem on Dec 28, 2007. Female patient, 38 years of age, weighting 115.0 lb, was diagnosed with arthropod bite, skin infection and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: coordination abnormal, decreased activity, dyskinesia, gait disturbance, memory impairment, neurological symptom, . AVELOX dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Vyvanse Side Effects Report #5597457-X
VYVANSE problem was reported by a Physician from UNITED STATES on Aug 28, 2007. Male patient, child 9 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with VYVANSE. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, decreased activity, . VYVANSE dosage: 30 MG, 1X/DAY:QD, ORAL. Patient recovered.
DECREASED ACTIVITY : Lipitor Side Effects Report #5524186-0
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on Nov 13, 2007. Female patient, weighting 179.9 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: abasia, decreased activity, impaired work ability, muscle spasms, myalgia, pain, pain in extremity, quality of life decreased, . LIPITOR dosage: unknown. During the same period patient was treated with TYLENOL, LISINOPRIL, PRILOSEC. Patient was hospitalized and became disabled. Patient recovered.
DECREASED ACTIVITY : Simvastatin Side Effects Report #5531465-X
SIMVASTATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 28, 2007. Male patient, 52 years of age, weighting 162.0 lb, was diagnosed with blood cholesterol increased and was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, decreased activity, fatigue, gait disturbance, . SIMVASTATIN dosage: 20 MG DAILY PO. Patient recovered.
DECREASED ACTIVITY : Byetta Side Effects Report #5578309-8
Consumer or non-health professional from UNITED STATES reported BYETTA problem on July 12, 2007. Male patient, 63 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 activity, depression, nausea, . BYETTA dosage: unknown. During the same period patient was treated with AMARYL, GLUCOPHAGE. Patient recovered.
DECREASED ACTIVITY : Alprazolam Side Effects Report #5473613-6
ALPRAZOLAM problem was reported by a Consumer or non-health professional from JAPAN on Sept 19, 2007. Male patient, weighting 8.40 lb, was treated with ALPRAZOLAM. After drug was administered, patient experienced the following problems/side effects: congenital anomaly, decreased activity, feeding disorder, muscular dystrophy, rhabdomyolysis, somnolence, stress, . ALPRAZOLAM dosage: unknown. During the same period patient was treated with DEPAS, LUDIOMIL. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Temodal Side Effects Report #5477391-6
Physician from JAPAN reported TEMODAL problem on Sept 26, 2007. Male patient, 83 years of age, weighting 90.39 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: anorexia, decreased activity, fungal infection, opportunistic infection, oral intake reduced, pneumonia, respiratory failure, . TEMODAL dosage: 150 MG/M2;QD;PO. During the same period patient was treated with PREDONINE, FAMOTIDINE, MUCOSTA, AMINO ACIDS, PENTCILLIN. Patient died on 11/15/2006.
DECREASED ACTIVITY : Nitric Side Effects Report #5477595-2
NITRIC OXIDE problem was reported by a Physician from SPAIN on Sept 27, 2007. Male patient, weighting 1.87 lb, was diagnosed with lung disorder and was treated with NITRIC OXIDE. After drug was administered, patient experienced the following problems/side effects: coagulopathy, decreased activity, intraventricular haemorrhage, patent ductus arteriosus, . NITRIC OXIDE dosage: unknown. During the same period patient was treated with AMPICILLIN, TOBRAMYCIN, INSULIN, PLASMA, BLOOD CELLS, VITAMIN K, FUROSEMIDE. Patient was hospitalized. Patient died on 01/09/2007.
DECREASED ACTIVITY : Nexium Side Effects Report #5489739-7
Consumer or non-health professional from CANADA reported NEXIUM problem on Oct 10, 2007. Female patient, 59 years of age, was diagnosed with nausea and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: cardiac disorder, decreased activity, dyspnoea, palpitations, yawning, . NEXIUM dosage: unknown. During the same period patient was treated with ELTROXIN, ADALAT, CYCLOSPORINE, AMITRIPTYLINE. Patient was hospitalized. Patient recovered.
DECREASED ACTIVITY : Lovastatin Side Effects Report #5496715-7
LOVASTATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 23, 2007. Male patient, weighting 180.0 lb, was diagnosed with blood cholesterol increased and was treated with LOVASTATIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, decreased activity, myalgia, pain in extremity, paraesthesia, rash, . LOVASTATIN dosage: 400MG 1 PER DAY PO. Patient recovered.
DECREASED ACTIVITY : Chantix Side Effects Report #5498023-7
Physician from UNITED STATES reported CHANTIX problem on Oct 13, 2007. Female patient, weighting 162.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: asthenia, decreased activity, decreased appetite, dizziness, head discomfort, hyperaesthesia, malaise, nausea, . CHANTIX dosage: unknown. During the same period patient was treated with ACTOS, METFORMIN, GLYBURIDE, AZULFIDINE, ACETYLSALICYLIC ACID SRT. Patient recovered.
DECREASED ACTIVITY : Zyrtec Side Effects Report #5498608-8
ZYRTEC problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 25, 2007. Female patient, child 7 years of age, weighting 58.00 lb, was diagnosed with hypersensitivity and was treated with ZYRTEC. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, decreased activity, pain in extremity, . ZYRTEC dosage: unknown. Patient recovered.
DECREASED ACTIVITY : Fluoxetine Side Effects Report #5445824-7
Health Professional from TURKEY reported FLUOXETINE problem on Aug 20, 2007. Female patient, 13 years of age, was diagnosed with obsessive-compulsive disorder and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, decreased activity, decreased appetite, echolalia, hypersomnia, obsessive-compulsive disorder, psychotic disorder, self injurious behaviour, . FLUOXETINE dosage: 10 MG, QD, 30 MG QD. During the same period patient was treated with RISPERIDONE. Patient recovered.
DECREASED ACTIVITY : Chantix Side Effects Report #5466222-6
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 12, 2007. Female patient, weighting 162.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: asthenia, decreased activity, decreased appetite, dizziness, head discomfort, hyperaesthesia, malaise, nausea, . CHANTIX dosage: unknown. During the same period patient was treated with ACTOS, METFORMIN, GLYBURIDE, AZULFIDINE, ASPIRIN. Patient recovered.
DECREASED ACTIVITY : Humira Side Effects Report #5471163-4
Pharmacist from FRANCE reported HUMIRA problem on Sept 18, 2007. Female patient, weighting 119.9 lb, was diagnosed with rheumatoid arthritis, spondylitis, antibiotic prophylaxis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: burning sensation, decreased activity, fatigue, hypotension, malaise, pain, pyrexia, sensory disturbance, . HUMIRA dosage: unknown. During the same period patient was treated with RIFINAH. Patient recovered.