Please choose an event type to view the corresponding MedsFacts report:

CONSTIPATION ( 5 FDA reports)
CONVULSION ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE INCREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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