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

DRUG INEFFECTIVE ( 191 FDA reports)
NAUSEA ( 151 FDA reports)
PAIN ( 136 FDA reports)
VOMITING ( 120 FDA reports)
DIARRHOEA ( 97 FDA reports)
HEADACHE ( 95 FDA reports)
DRUG DIVERSION ( 94 FDA reports)
WITHDRAWAL SYNDROME ( 80 FDA reports)
ANXIETY ( 77 FDA reports)
OVERDOSE ( 75 FDA reports)
INSOMNIA ( 73 FDA reports)
CONSTIPATION ( 68 FDA reports)
DEATH ( 68 FDA reports)
DEPRESSION ( 63 FDA reports)
WEIGHT DECREASED ( 63 FDA reports)
DYSPNOEA ( 62 FDA reports)
FALL ( 56 FDA reports)
OEDEMA PERIPHERAL ( 56 FDA reports)
FATIGUE ( 55 FDA reports)
HYPERHIDROSIS ( 54 FDA reports)
DRUG EFFECT DECREASED ( 53 FDA reports)
CHEST PAIN ( 51 FDA reports)
DIZZINESS ( 50 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 50 FDA reports)
DEHYDRATION ( 49 FDA reports)
MALAISE ( 49 FDA reports)
BACK PAIN ( 48 FDA reports)
LOSS OF CONSCIOUSNESS ( 48 FDA reports)
SOMNOLENCE ( 48 FDA reports)
PNEUMONIA ( 46 FDA reports)
MENTAL STATUS CHANGES ( 43 FDA reports)
CONFUSIONAL STATE ( 41 FDA reports)
MEMORY IMPAIRMENT ( 41 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 39 FDA reports)
PAIN IN EXTREMITY ( 39 FDA reports)
RASH ( 39 FDA reports)
CARDIO-RESPIRATORY ARREST ( 38 FDA reports)
PYREXIA ( 38 FDA reports)
HYPOAESTHESIA ( 36 FDA reports)
HALLUCINATION ( 35 FDA reports)
TREMOR ( 35 FDA reports)
ABDOMINAL PAIN UPPER ( 34 FDA reports)
ARTHRALGIA ( 34 FDA reports)
ACCIDENTAL OVERDOSE ( 33 FDA reports)
ANAEMIA ( 33 FDA reports)
HYPERTENSION ( 32 FDA reports)
OSTEOARTHRITIS ( 32 FDA reports)
ABDOMINAL PAIN ( 31 FDA reports)
CONTUSION ( 31 FDA reports)
DIABETES MELLITUS ( 31 FDA reports)
URINARY TRACT INFECTION ( 31 FDA reports)
ASTHENIA ( 30 FDA reports)
BONE DISORDER ( 30 FDA reports)
INTENTIONAL DRUG MISUSE ( 30 FDA reports)
MUSCULAR WEAKNESS ( 30 FDA reports)
FEELING ABNORMAL ( 29 FDA reports)
VISION BLURRED ( 29 FDA reports)
BREAKTHROUGH PAIN ( 28 FDA reports)
HYPOTENSION ( 28 FDA reports)
WEIGHT INCREASED ( 27 FDA reports)
COMA ( 26 FDA reports)
IMPAIRED HEALING ( 26 FDA reports)
ROAD TRAFFIC ACCIDENT ( 26 FDA reports)
ABDOMINAL DISCOMFORT ( 25 FDA reports)
ASTHMA ( 25 FDA reports)
INJURY ( 25 FDA reports)
RESPIRATORY DEPRESSION ( 25 FDA reports)
CEREBROVASCULAR ACCIDENT ( 24 FDA reports)
CONVULSION ( 24 FDA reports)
DECREASED APPETITE ( 24 FDA reports)
LETHARGY ( 24 FDA reports)
MEDICATION ERROR ( 24 FDA reports)
MYALGIA ( 24 FDA reports)
PELVIC PAIN ( 24 FDA reports)
SUICIDAL IDEATION ( 24 FDA reports)
OSTEOMYELITIS ( 23 FDA reports)
RENAL FAILURE ( 23 FDA reports)
BLOOD PRESSURE INCREASED ( 22 FDA reports)
DYSKINESIA ( 22 FDA reports)
MASS ( 22 FDA reports)
OSTEONECROSIS OF JAW ( 22 FDA reports)
PRURITUS ( 22 FDA reports)
SEPSIS ( 22 FDA reports)
SWELLING FACE ( 22 FDA reports)
TOOTH EXTRACTION ( 22 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 21 FDA reports)
DRUG DEPENDENCE ( 21 FDA reports)
EMOTIONAL DISTRESS ( 21 FDA reports)
METASTASES TO BONE ( 21 FDA reports)
MULTIPLE DRUG OVERDOSE ( 21 FDA reports)
OSTEOPENIA ( 21 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
VAGINAL HAEMORRHAGE ( 21 FDA reports)
COMPLETED SUICIDE ( 20 FDA reports)
PALPITATIONS ( 20 FDA reports)
THINKING ABNORMAL ( 20 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 20 FDA reports)
MENTAL DISORDER ( 19 FDA reports)
OEDEMA ( 19 FDA reports)
DRUG HYPERSENSITIVITY ( 18 FDA reports)
MIGRAINE ( 18 FDA reports)
MITRAL VALVE INCOMPETENCE ( 18 FDA reports)
RESPIRATORY FAILURE ( 18 FDA reports)
CELLULITIS ( 17 FDA reports)
DENTAL CARIES ( 17 FDA reports)
MUSCLE SPASMS ( 17 FDA reports)
PARAESTHESIA ( 17 FDA reports)
SINUSITIS ( 17 FDA reports)
SWELLING ( 17 FDA reports)
ANGER ( 16 FDA reports)
CONDITION AGGRAVATED ( 16 FDA reports)
CRYING ( 16 FDA reports)
DISORIENTATION ( 16 FDA reports)
DRUG ABUSE ( 16 FDA reports)
DYSARTHRIA ( 16 FDA reports)
DYSURIA ( 16 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
METASTASES TO LUNG ( 16 FDA reports)
NEUROPATHY PERIPHERAL ( 16 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 16 FDA reports)
PULMONARY EMBOLISM ( 16 FDA reports)
SHOCK ( 16 FDA reports)
STRESS ( 16 FDA reports)
STUPOR ( 16 FDA reports)
SURGERY ( 16 FDA reports)
ANHEDONIA ( 15 FDA reports)
ARTERIOSCLEROSIS ( 15 FDA reports)
ATRIAL FIBRILLATION ( 15 FDA reports)
DEAFNESS ( 15 FDA reports)
DRUG PRESCRIBING ERROR ( 15 FDA reports)
ENCEPHALOPATHY ( 15 FDA reports)
INFECTION ( 15 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 15 FDA reports)
MOBILITY DECREASED ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
AGITATION ( 14 FDA reports)
BALANCE DISORDER ( 14 FDA reports)
CAROTID ARTERY STENOSIS ( 14 FDA reports)
CHILLS ( 14 FDA reports)
CHOLECYSTECTOMY ( 14 FDA reports)
DYSPHAGIA ( 14 FDA reports)
GASTRITIS ( 14 FDA reports)
INTESTINAL OBSTRUCTION ( 14 FDA reports)
NECK PAIN ( 14 FDA reports)
NERVOUSNESS ( 14 FDA reports)
VIRAL INFECTION ( 14 FDA reports)
AMNESIA ( 13 FDA reports)
BONE PAIN ( 13 FDA reports)
CEREBRAL ATROPHY ( 13 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 13 FDA reports)
COGNITIVE DISORDER ( 13 FDA reports)
DISTURBANCE IN ATTENTION ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
ESCHERICHIA INFECTION ( 13 FDA reports)
EYE DISORDER ( 13 FDA reports)
HAEMATOMA ( 13 FDA reports)
HAEMATURIA ( 13 FDA reports)
INCONTINENCE ( 13 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 13 FDA reports)
OBESITY ( 13 FDA reports)
ORAL CANDIDIASIS ( 13 FDA reports)
PERIPHERAL ISCHAEMIA ( 13 FDA reports)
POLLAKIURIA ( 13 FDA reports)
SKIN LACERATION ( 13 FDA reports)
SLEEP APNOEA SYNDROME ( 13 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
ABSCESS DRAINAGE ( 12 FDA reports)
ABSCESS ORAL ( 12 FDA reports)
AFFECTIVE DISORDER ( 12 FDA reports)
ARTERIAL BYPASS OPERATION ( 12 FDA reports)
BLADDER PROLAPSE ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
BONE FISTULA ( 12 FDA reports)
BONE LESION ( 12 FDA reports)
CATHETERISATION VENOUS ( 12 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 12 FDA reports)
COLOSTOMY ( 12 FDA reports)
COMPRESSION FRACTURE ( 12 FDA reports)
COUGH ( 12 FDA reports)
DEBRIDEMENT ( 12 FDA reports)
DENTAL IMPLANTATION ( 12 FDA reports)
DEVICE FAILURE ( 12 FDA reports)
DRUG INTOLERANCE ( 12 FDA reports)
DRUG TOXICITY ( 12 FDA reports)
DYSAESTHESIA ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
ETHMOID SINUS SURGERY ( 12 FDA reports)
FAECAL INCONTINENCE ( 12 FDA reports)
FEELING JITTERY ( 12 FDA reports)
FEMORAL ARTERY OCCLUSION ( 12 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 12 FDA reports)
GOITRE ( 12 FDA reports)
HYPERTONIC BLADDER ( 12 FDA reports)
INFLUENZA LIKE ILLNESS ( 12 FDA reports)
INTERMITTENT CLAUDICATION ( 12 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 12 FDA reports)
MAXILLOFACIAL OPERATION ( 12 FDA reports)
MENINGIOMA ( 12 FDA reports)
METABOLIC ENCEPHALOPATHY ( 12 FDA reports)
METASTATIC NEOPLASM ( 12 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 12 FDA reports)
OSTEONECROSIS ( 12 FDA reports)
PELVIC ABSCESS ( 12 FDA reports)
PLASMAPHERESIS ( 12 FDA reports)
PROLAPSE REPAIR ( 12 FDA reports)
RECTAL PROLAPSE ( 12 FDA reports)
SEDATION ( 12 FDA reports)
SINUS ANTROSTOMY ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
UTEROVAGINAL PROLAPSE ( 12 FDA reports)
WOUND DECOMPOSITION ( 12 FDA reports)
WOUND SECRETION ( 12 FDA reports)
ABASIA ( 11 FDA reports)
ADVERSE DRUG REACTION ( 11 FDA reports)
ATELECTASIS ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
DEPRESSED MOOD ( 11 FDA reports)
DYSGEUSIA ( 11 FDA reports)
DYSPHONIA ( 11 FDA reports)
EMPHYSEMA ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
HYPERSOMNIA ( 11 FDA reports)
HYPOTHYROIDISM ( 11 FDA reports)
INTENTIONAL OVERDOSE ( 11 FDA reports)
LYMPHADENOPATHY ( 11 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 11 FDA reports)
NIGHTMARE ( 11 FDA reports)
PNEUMONIA ASPIRATION ( 11 FDA reports)
POSTNASAL DRIP ( 11 FDA reports)
RASH GENERALISED ( 11 FDA reports)
RESTLESS LEGS SYNDROME ( 11 FDA reports)
RHABDOMYOLYSIS ( 11 FDA reports)
SUICIDE ATTEMPT ( 11 FDA reports)
TYPE 2 DIABETES MELLITUS ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
ABNORMAL DREAMS ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 10 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
ANOREXIA ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BRAIN INJURY ( 10 FDA reports)
BRAIN OEDEMA ( 10 FDA reports)
BURNING SENSATION ( 10 FDA reports)
CYANOSIS ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DISABILITY ( 10 FDA reports)
DRUG ABUSER ( 10 FDA reports)
DRY MOUTH ( 10 FDA reports)
DUANE'S SYNDROME ( 10 FDA reports)
EMOTIONAL DISORDER ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
IMPAIRED WORK ABILITY ( 10 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
NEUROGENIC BLADDER ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
SINUS HEADACHE ( 10 FDA reports)
SUBSTANCE ABUSE ( 10 FDA reports)
TENDON DISORDER ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
TINNITUS ( 10 FDA reports)
WRIST FRACTURE ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 9 FDA reports)
ADVERSE EVENT ( 9 FDA reports)
AORTIC VALVE INCOMPETENCE ( 9 FDA reports)
ARTHRITIS ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
CARPAL TUNNEL SYNDROME ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
DRUG DOSE OMISSION ( 9 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
DYSPAREUNIA ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
GAIT DISTURBANCE ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HOSTILITY ( 9 FDA reports)
HOT FLUSH ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
METASTASIS ( 9 FDA reports)
MOOD SWINGS ( 9 FDA reports)
MUSCLE TWITCHING ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 9 FDA reports)
RADIOTHERAPY ( 9 FDA reports)
SCAR ( 9 FDA reports)
SKIN DISORDER ( 9 FDA reports)
SWOLLEN TONGUE ( 9 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 9 FDA reports)
TREATMENT NONCOMPLIANCE ( 9 FDA reports)
ABDOMINAL ADHESIONS ( 8 FDA reports)
BIOPSY BLADDER ABNORMAL ( 8 FDA reports)
BIOPSY SKIN ABNORMAL ( 8 FDA reports)
BONE EROSION ( 8 FDA reports)
BONE SCAN ABNORMAL ( 8 FDA reports)
COSTOCHONDRITIS ( 8 FDA reports)
DELUSION ( 8 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
FEMORAL NECK FRACTURE ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
FORMICATION ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
GINGIVAL BLEEDING ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
HIATUS HERNIA ( 8 FDA reports)
HIP FRACTURE ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 8 FDA reports)
IMPAIRED DRIVING ABILITY ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
MICTURITION URGENCY ( 8 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 8 FDA reports)
OVARIAN ADHESION ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PELVIC ADHESIONS ( 8 FDA reports)
POSTURE ABNORMAL ( 8 FDA reports)
PULMONARY MASS ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
RIB FRACTURE ( 8 FDA reports)
SALPINGITIS ( 8 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 8 FDA reports)
SPINAL FRACTURE ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 8 FDA reports)
TOOTH DISORDER ( 8 FDA reports)
UNEVALUABLE EVENT ( 8 FDA reports)
VISUAL IMPAIRMENT ( 8 FDA reports)
WEIGHT FLUCTUATION ( 8 FDA reports)
ABSCESS ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BEDRIDDEN ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
BONE DEBRIDEMENT ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 7 FDA reports)
CLAUSTROPHOBIA ( 7 FDA reports)
DIFFICULTY IN WALKING ( 7 FDA reports)
ECONOMIC PROBLEM ( 7 FDA reports)
EJECTION FRACTION DECREASED ( 7 FDA reports)
EUPHORIC MOOD ( 7 FDA reports)
FLUID REPLACEMENT ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
GASTRIC DISORDER ( 7 FDA reports)
GRIEF REACTION ( 7 FDA reports)
HERNIA ( 7 FDA reports)
HOSPITALISATION ( 7 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 7 FDA reports)
HYPOVENTILATION ( 7 FDA reports)
ILEUS ( 7 FDA reports)
IMPAIRED REASONING ( 7 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 7 FDA reports)
LACERATION ( 7 FDA reports)
LOOSE TOOTH ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
MASS EXCISION ( 7 FDA reports)
MOANING ( 7 FDA reports)
MOOD ALTERED ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
MULTIPLE INJURIES ( 7 FDA reports)
MULTIPLE SCLEROSIS ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
PANIC DISORDER ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
SELF-MEDICATION ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SPINAL DECOMPRESSION ( 7 FDA reports)
SPONDYLOLISTHESIS ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
TONGUE HAEMORRHAGE ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BLADDER DISCOMFORT ( 6 FDA reports)
BLEPHARITIS ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BUNDLE BRANCH BLOCK ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 6 FDA reports)
CHOKING ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
CORNEAL ABRASION ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DECREASED INTEREST ( 6 FDA reports)
DERMATITIS ( 6 FDA reports)
DIPLOPIA ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
INADEQUATE ANALGESIA ( 6 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 6 FDA reports)
JOINT CONTRACTURE ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
MOTOR DYSFUNCTION ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
NARCOTIC INTOXICATION ( 6 FDA reports)
NECK INJURY ( 6 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 6 FDA reports)
NEUROPATHIC ARTHROPATHY ( 6 FDA reports)
OSTEOCHONDROMA ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
RASH VESICULAR ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SEXUAL DYSFUNCTION ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
SKIN HYPERTROPHY ( 6 FDA reports)
SKIN INDURATION ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
STASIS DERMATITIS ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
VENTRICULAR HYPOKINESIA ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
ANXIETY DISORDER ( 5 FDA reports)
AORTIC CALCIFICATION ( 5 FDA reports)
ARTHROPATHY ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BONE LOSS ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
COLONIC POLYP ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
FRUSTRATION ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATIC LESION ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
IMPAIRED SELF-CARE ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NEUROPATHY ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
OVARIAN CYST ( 5 FDA reports)
PARAESTHESIA ORAL ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BURN INFECTION ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DRUG TOLERANCE ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
FEAR ( 4 FDA reports)
FISTULA DISCHARGE ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HIP ARTHROPLASTY ( 4 FDA reports)
HYPERAESTHESIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
JOINT INJURY ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MEDICATION RESIDUE ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
OSTEITIS DEFORMANS ( 4 FDA reports)
PERIODONTAL DISEASE ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PHYSICAL DISABILITY ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PRECANCEROUS CELLS PRESENT ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SPERM COUNT DECREASED ( 4 FDA reports)
SYNOVIAL CYST ( 4 FDA reports)
TOOTH INFECTION ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
ULNAR NERVE INJURY ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
ENURESIS ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
GROWING PAINS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HORDEOLUM ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
IUD MIGRATION ( 3 FDA reports)
JAW DISORDER ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
NAIL DISCOMFORT ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OTITIS EXTERNA ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POST PROCEDURAL DISCOMFORT ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
REACTION TO PRESERVATIVES ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
SACROILIITIS ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
SPINAL FUSION SURGERY ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
UTERINE DISORDER ( 3 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 3 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ACQUIRED HYDROCELE ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
COUGH DECREASED ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOGONADISM ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYELOMALACIA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OESOPHAGEAL OPERATION ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREMATURE EJACULATION ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SECONDARY HYPOGONADISM ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TENSION ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETERIC CANCER METASTATIC ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DETOXIFICATION ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACTOR VII DEFICIENCY ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERMETABOLISM ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE RUPTURE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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