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

DYSPNOEA ( 71 FDA reports)
DRUG DEPENDENCE ( 49 FDA reports)
ANXIETY ( 44 FDA reports)
PAIN ( 43 FDA reports)
SINUSITIS ( 38 FDA reports)
HEADACHE ( 37 FDA reports)
NASAL CONGESTION ( 35 FDA reports)
NAUSEA ( 33 FDA reports)
ABDOMINAL PAIN ( 31 FDA reports)
COUGH ( 31 FDA reports)
OSTEOMYELITIS ( 31 FDA reports)
OSTEONECROSIS OF JAW ( 31 FDA reports)
DEPRESSION ( 29 FDA reports)
DIZZINESS ( 29 FDA reports)
PYREXIA ( 29 FDA reports)
SINUS DISORDER ( 28 FDA reports)
FATIGUE ( 27 FDA reports)
PRIMARY SEQUESTRUM ( 26 FDA reports)
PAIN IN EXTREMITY ( 25 FDA reports)
ABSCESS ( 24 FDA reports)
METASTASES TO BONE ( 24 FDA reports)
PARAESTHESIA ( 24 FDA reports)
PNEUMONIA ( 24 FDA reports)
BONE DISORDER ( 23 FDA reports)
DIARRHOEA ( 23 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
OSTEOARTHRITIS ( 23 FDA reports)
VOMITING ( 23 FDA reports)
ARTHRITIS ( 22 FDA reports)
BACK PAIN ( 22 FDA reports)
CHEST PAIN ( 22 FDA reports)
DYSGEUSIA ( 22 FDA reports)
INJURY ( 22 FDA reports)
ASTHENIA ( 21 FDA reports)
DENTAL CARIES ( 21 FDA reports)
LUNG INFILTRATION ( 21 FDA reports)
EPISTAXIS ( 20 FDA reports)
FALL ( 20 FDA reports)
PALPITATIONS ( 20 FDA reports)
SWELLING FACE ( 20 FDA reports)
ANOSMIA ( 19 FDA reports)
ARTHRALGIA ( 19 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
GINGIVAL ULCERATION ( 19 FDA reports)
MYOCARDIAL INFARCTION ( 19 FDA reports)
ORAL DISORDER ( 19 FDA reports)
ORAL PAIN ( 19 FDA reports)
PURULENCE ( 19 FDA reports)
VISION BLURRED ( 19 FDA reports)
ABDOMINAL PAIN UPPER ( 18 FDA reports)
BLOOD PRESSURE INCREASED ( 18 FDA reports)
BREAST CANCER RECURRENT ( 18 FDA reports)
DIVERTICULUM ( 18 FDA reports)
HYPERTENSION ( 18 FDA reports)
MUSCULOSKELETAL PAIN ( 18 FDA reports)
TOOTHACHE ( 18 FDA reports)
INFLAMMATION ( 17 FDA reports)
RHINORRHOEA ( 17 FDA reports)
SENSITIVITY OF TEETH ( 17 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 16 FDA reports)
CONSTIPATION ( 16 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 16 FDA reports)
HEPATITIS B ( 16 FDA reports)
HEPATITIS C ( 16 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 16 FDA reports)
MITRAL VALVE INCOMPETENCE ( 16 FDA reports)
URINARY TRACT INFECTION ( 16 FDA reports)
AGEUSIA ( 15 FDA reports)
ANAEMIA ( 15 FDA reports)
INSOMNIA ( 15 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 15 FDA reports)
CHOLELITHIASIS ( 14 FDA reports)
CONFUSIONAL STATE ( 14 FDA reports)
FISTULA ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
INFECTION ( 14 FDA reports)
MALAISE ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
TOOTH EXTRACTION ( 14 FDA reports)
BASAL CELL CARCINOMA ( 13 FDA reports)
BRONCHITIS ( 13 FDA reports)
CAROTID ARTERY STENOSIS ( 13 FDA reports)
COLONIC POLYP ( 13 FDA reports)
HEPATIC CYST ( 13 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 13 FDA reports)
MIGRAINE ( 13 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
PHARYNGITIS ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
POOR QUALITY SLEEP ( 13 FDA reports)
PULMONARY EMBOLISM ( 13 FDA reports)
RASH PRURITIC ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
TOOTH INFECTION ( 13 FDA reports)
ASTHMA ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BONE LESION ( 12 FDA reports)
CATARACT ( 12 FDA reports)
CONTUSION ( 12 FDA reports)
DEEP VEIN THROMBOSIS ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
GINGIVAL SWELLING ( 12 FDA reports)
HAEMORRHOIDS ( 12 FDA reports)
HYPERLIPIDAEMIA ( 12 FDA reports)
IMPAIRED HEALING ( 12 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
MONOCYTE COUNT INCREASED ( 12 FDA reports)
PRESYNCOPE ( 12 FDA reports)
RASH ( 12 FDA reports)
RENAL CYST ( 12 FDA reports)
SINUS HEADACHE ( 12 FDA reports)
SPINAL OSTEOARTHRITIS ( 12 FDA reports)
TENDERNESS ( 12 FDA reports)
TREMOR ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 11 FDA reports)
BONE SCAN ABNORMAL ( 11 FDA reports)
BURSITIS ( 11 FDA reports)
CLAVICLE FRACTURE ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 11 FDA reports)
CORONARY ARTERY DISEASE ( 11 FDA reports)
CYST ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DILATATION VENTRICULAR ( 11 FDA reports)
GLAUCOMA ( 11 FDA reports)
HAEMATURIA ( 11 FDA reports)
HYDRONEPHROSIS ( 11 FDA reports)
HYPERCHOLESTEROLAEMIA ( 11 FDA reports)
HYPERHIDROSIS ( 11 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 11 FDA reports)
LYMPHOEDEMA ( 11 FDA reports)
MALIGNANT MELANOMA IN SITU ( 11 FDA reports)
MEMORY IMPAIRMENT ( 11 FDA reports)
MOOD SWINGS ( 11 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 11 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 11 FDA reports)
NECROSIS ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
RIB FRACTURE ( 11 FDA reports)
ROTATOR CUFF SYNDROME ( 11 FDA reports)
SINUS POLYP DEGENERATION ( 11 FDA reports)
SLEEP APNOEA SYNDROME ( 11 FDA reports)
SPINAL DISORDER ( 11 FDA reports)
TOOTH DISORDER ( 11 FDA reports)
UPPER LIMB FRACTURE ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 11 FDA reports)
VITREOUS DETACHMENT ( 11 FDA reports)
ABSCESS DRAINAGE ( 10 FDA reports)
BRONCHIOLITIS ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
DEPENDENCE ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HYPERSENSITIVITY ( 10 FDA reports)
LYMPHADENOPATHY ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
TOOTH ABSCESS ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
DEAFNESS ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
DYSPNOEA EXERTIONAL ( 9 FDA reports)
FACIAL PAIN ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
MASTITIS ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
VITREOUS FLOATERS ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
ANGER ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
DEATH ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
LARYNGEAL OEDEMA ( 8 FDA reports)
MASS ( 8 FDA reports)
MOUTH CYST ( 8 FDA reports)
MOUTH HAEMORRHAGE ( 8 FDA reports)
MUCOSAL ATROPHY ( 8 FDA reports)
OROANTRAL FISTULA ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
PROTEIN TOTAL DECREASED ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
PURULENT DISCHARGE ( 8 FDA reports)
RENAL MASS ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 8 FDA reports)
WOUND DEHISCENCE ( 8 FDA reports)
ARTHROPATHY ( 7 FDA reports)
BLOOD CALCIUM INCREASED ( 7 FDA reports)
BLOOD IRON DECREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
DEBRIDEMENT ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEVICE MALFUNCTION ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
ETHMOID SINUS SURGERY ( 7 FDA reports)
FEELING COLD ( 7 FDA reports)
GINGIVAL PAIN ( 7 FDA reports)
HAEMANGIOMA OF LIVER ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HYPOVENTILATION ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
JOINT SPRAIN ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
OPEN WOUND ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
RECTAL FISSURE ( 7 FDA reports)
REFLUX OESOPHAGITIS ( 7 FDA reports)
RHINITIS ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SINUS ANTROSTOMY ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
STRESS ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
UTERINE LEIOMYOMA ( 7 FDA reports)
WALKING AID USER ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BONE NEOPLASM MALIGNANT ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
EAR CONGESTION ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
ENDOMETRIAL CANCER ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
HYPERMETABOLISM ( 6 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
METASTASES TO LIVER ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NERVE ROOT COMPRESSION ( 6 FDA reports)
OSTEOLYSIS ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
REBOUND EFFECT ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SKIN PAPILLOMA ( 6 FDA reports)
SPONDYLOLISTHESIS ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
SWELLING ( 6 FDA reports)
TALIPES ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 6 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
ADRENAL MASS ( 5 FDA reports)
AGITATION ( 5 FDA reports)
ALVEOLAR OSTEITIS ( 5 FDA reports)
ALVEOLOPLASTY ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
BRUXISM ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FRONTAL SINUS OPERATION ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GINGIVAL ERYTHEMA ( 5 FDA reports)
GINGIVAL INFECTION ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
JAW LESION EXCISION ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
MUSCLE STRAIN ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NASAL SEPTAL OPERATION ( 5 FDA reports)
OBESITY ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
RADIUS FRACTURE ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RETINOPATHY ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
SEASONAL ALLERGY ( 5 FDA reports)
SPHENOID SINUS OPERATION ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TOOTH INJURY ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
WALKING DISABILITY ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 4 FDA reports)
APHASIA ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BURNOUT SYNDROME ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
EPIGASTRIC DISCOMFORT ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FEAR ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTRODUODENITIS ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GENITAL HERPES ( 4 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NASAL MUCOSAL DISORDER ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
NODULE ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HORNER'S SYNDROME ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
POLYP COLORECTAL ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VAGINAL FISTULA ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANKLE RECONSTRUCTION ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CAROTID ARTERY DISEASE ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DIVERTICULAR HERNIA ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
EYELID OPERATION ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPHOCYTOTOXIC ANTIBODY POSITIVE ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MAXILLOFACIAL OPERATION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATIC OBSTRUCTION ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ULCER ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUSTACHIAN TUBE STENOSIS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRANASAL HYPOAESTHESIA ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL NECROSIS ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASAL VESTIBULITIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICOLOGIC TEST ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TRAUMATIC OCCLUSION ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VOLUNTARY REDUNDANCY ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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