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

DEPRESSION ( 26 FDA reports)
DRUG DEPENDENCE ( 26 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 26 FDA reports)
ANXIETY ( 25 FDA reports)
PAIN ( 25 FDA reports)
CONSTIPATION ( 22 FDA reports)
ASTHENIA ( 18 FDA reports)
OEDEMA PERIPHERAL ( 18 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 17 FDA reports)
CHEST DISCOMFORT ( 16 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 16 FDA reports)
DYSPEPSIA ( 15 FDA reports)
PARANOIA ( 15 FDA reports)
DYSPNOEA ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
BRONCHITIS ACUTE ( 13 FDA reports)
NASAL CONGESTION ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
COUGH ( 12 FDA reports)
DRUG TOLERANCE ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
DYSPNOEA EXERTIONAL ( 12 FDA reports)
INSOMNIA ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
ARTHRALGIA ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
EAR PAIN ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
INADEQUATE ANALGESIA ( 9 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 9 FDA reports)
JOINT SPRAIN ( 9 FDA reports)
NIGHTMARE ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
SKIN LESION ( 9 FDA reports)
SLEEP DISORDER ( 9 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
DISTURBANCE IN ATTENTION ( 8 FDA reports)
FALL ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
NON-CARDIAC CHEST PAIN ( 8 FDA reports)
POLLAKIURIA ( 8 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
TREMOR ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ANHEDONIA ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BEREAVEMENT REACTION ( 7 FDA reports)
BLEPHARITIS ( 7 FDA reports)
DEPRESSED MOOD ( 7 FDA reports)
DRY EYE ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
ONYCHOMYCOSIS ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
PROSTATITIS ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
SELF ESTEEM DECREASED ( 7 FDA reports)
SNORING ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
JOINT EFFUSION ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
NOCTURIA ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
POSTOPERATIVE CONSTIPATION ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
URINE FLOW DECREASED ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MICTURITION URGENCY ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BRONCHIAL HYPERACTIVITY ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
UTERINE PERFORATION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
COMA ( 3 FDA reports)
CRYING ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOGONADISM ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OTITIS MEDIA CHRONIC ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
VITAMIN B12 DEFICIENCY ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
APHONIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BASE EXCESS INCREASED ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYRINGOPLASTY ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEURODERMATITIS ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SCAB ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
ULCER ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)