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

DRUG DEPENDENCE ( 13 FDA reports)
DEPRESSION ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
PAIN ( 11 FDA reports)
ANXIETY ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
MOOD ALTERED ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
THINKING ABNORMAL ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CRYING ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
DRUG TOLERANCE ( 7 FDA reports)
DYSTHYMIC DISORDER ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PLANTAR FASCIITIS ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
TARSAL TUNNEL SYNDROME ( 7 FDA reports)
TREMOR ( 7 FDA reports)
ABDOMINAL ADHESIONS ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
INADEQUATE ANALGESIA ( 6 FDA reports)
RASH ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
POST PROCEDURAL OEDEMA ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SWELLING ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AGITATION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
NEUROPATHIC PAIN ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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