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

ARTHRALGIA ( 1903 FDA reports)
PAIN ( 1356 FDA reports)
HOT FLUSH ( 1127 FDA reports)
FATIGUE ( 1001 FDA reports)
ANXIETY ( 956 FDA reports)
PAIN IN EXTREMITY ( 846 FDA reports)
NAUSEA ( 839 FDA reports)
BACK PAIN ( 829 FDA reports)
OSTEONECROSIS OF JAW ( 792 FDA reports)
DYSPNOEA ( 776 FDA reports)
OSTEONECROSIS ( 765 FDA reports)
BONE DISORDER ( 761 FDA reports)
DEPRESSION ( 699 FDA reports)
HEADACHE ( 696 FDA reports)
ASTHENIA ( 695 FDA reports)
FALL ( 682 FDA reports)
TOOTH EXTRACTION ( 673 FDA reports)
INSOMNIA ( 655 FDA reports)
PAIN IN JAW ( 633 FDA reports)
BONE PAIN ( 631 FDA reports)
DIARRHOEA ( 612 FDA reports)
HYPOAESTHESIA ( 609 FDA reports)
OEDEMA PERIPHERAL ( 608 FDA reports)
OSTEOARTHRITIS ( 605 FDA reports)
DIZZINESS ( 600 FDA reports)
INJURY ( 594 FDA reports)
WEIGHT DECREASED ( 593 FDA reports)
ANAEMIA ( 573 FDA reports)
OSTEOMYELITIS ( 561 FDA reports)
WEIGHT INCREASED ( 558 FDA reports)
METASTASES TO BONE ( 550 FDA reports)
ALOPECIA ( 525 FDA reports)
ARTHRITIS ( 499 FDA reports)
IMPAIRED HEALING ( 493 FDA reports)
GAIT DISTURBANCE ( 487 FDA reports)
HYPERTENSION ( 485 FDA reports)
PYREXIA ( 477 FDA reports)
VOMITING ( 471 FDA reports)
NEOPLASM MALIGNANT ( 459 FDA reports)
PARAESTHESIA ( 456 FDA reports)
COUGH ( 444 FDA reports)
CONSTIPATION ( 425 FDA reports)
OSTEOPOROSIS ( 421 FDA reports)
MALAISE ( 413 FDA reports)
MYALGIA ( 411 FDA reports)
OSTEOPENIA ( 402 FDA reports)
NEUROPATHY PERIPHERAL ( 398 FDA reports)
PLEURAL EFFUSION ( 396 FDA reports)
DEATH ( 374 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 365 FDA reports)
SPINAL OSTEOARTHRITIS ( 359 FDA reports)
DECREASED APPETITE ( 355 FDA reports)
RASH ( 347 FDA reports)
CHEST PAIN ( 343 FDA reports)
INFECTION ( 343 FDA reports)
URINARY TRACT INFECTION ( 343 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 342 FDA reports)
BREAST CANCER ( 335 FDA reports)
MUSCLE SPASMS ( 334 FDA reports)
TOOTH DISORDER ( 332 FDA reports)
ANHEDONIA ( 324 FDA reports)
MUSCULOSKELETAL PAIN ( 322 FDA reports)
EMOTIONAL DISTRESS ( 318 FDA reports)
ABDOMINAL PAIN ( 315 FDA reports)
SWELLING ( 310 FDA reports)
TOOTHACHE ( 296 FDA reports)
MUSCULAR WEAKNESS ( 289 FDA reports)
DENTAL CARIES ( 288 FDA reports)
METASTASES TO LIVER ( 284 FDA reports)
PNEUMONIA ( 278 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 275 FDA reports)
BONE LESION ( 272 FDA reports)
SINUSITIS ( 269 FDA reports)
TOOTH LOSS ( 262 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 258 FDA reports)
NECK PAIN ( 257 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 256 FDA reports)
DEHYDRATION ( 250 FDA reports)
DEEP VEIN THROMBOSIS ( 247 FDA reports)
PRIMARY SEQUESTRUM ( 243 FDA reports)
ARTHROPATHY ( 237 FDA reports)
CELLULITIS ( 228 FDA reports)
BRONCHITIS ( 227 FDA reports)
HIATUS HERNIA ( 227 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 226 FDA reports)
PRURITUS ( 225 FDA reports)
DRUG DOSE OMISSION ( 222 FDA reports)
LUNG NEOPLASM ( 220 FDA reports)
CARPAL TUNNEL SYNDROME ( 216 FDA reports)
CATARACT ( 216 FDA reports)
DRY MOUTH ( 216 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 216 FDA reports)
ATELECTASIS ( 212 FDA reports)
LYMPHADENOPATHY ( 211 FDA reports)
INFLAMMATION ( 209 FDA reports)
NIGHT SWEATS ( 209 FDA reports)
VISION BLURRED ( 209 FDA reports)
ERYTHEMA ( 206 FDA reports)
BONE DENSITY DECREASED ( 205 FDA reports)
HAEMORRHOIDS ( 205 FDA reports)
RIB FRACTURE ( 205 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 203 FDA reports)
METASTASES TO SPINE ( 203 FDA reports)
DYSPHAGIA ( 202 FDA reports)
SURGERY ( 202 FDA reports)
HEPATIC STEATOSIS ( 199 FDA reports)
EXOSTOSIS ( 198 FDA reports)
BLOOD PRESSURE INCREASED ( 196 FDA reports)
CONFUSIONAL STATE ( 196 FDA reports)
JOINT SWELLING ( 193 FDA reports)
MEMORY IMPAIRMENT ( 193 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 192 FDA reports)
METASTASES TO LUNG ( 190 FDA reports)
FEELING ABNORMAL ( 189 FDA reports)
ORAL PAIN ( 188 FDA reports)
HYPERCHOLESTEROLAEMIA ( 187 FDA reports)
BURSITIS ( 185 FDA reports)
HYPERLIPIDAEMIA ( 184 FDA reports)
ABDOMINAL PAIN UPPER ( 183 FDA reports)
HYPOKALAEMIA ( 183 FDA reports)
PURULENT DISCHARGE ( 183 FDA reports)
BREAST CANCER RECURRENT ( 180 FDA reports)
DYSPEPSIA ( 180 FDA reports)
SCOLIOSIS ( 180 FDA reports)
SYNCOPE ( 180 FDA reports)
MOUTH ULCERATION ( 179 FDA reports)
LYMPHOEDEMA ( 178 FDA reports)
MITRAL VALVE INCOMPETENCE ( 178 FDA reports)
DISABILITY ( 176 FDA reports)
BLOOD GLUCOSE INCREASED ( 175 FDA reports)
DEFORMITY ( 175 FDA reports)
RENAL FAILURE ( 175 FDA reports)
ILL-DEFINED DISORDER ( 174 FDA reports)
FISTULA ( 173 FDA reports)
SWELLING FACE ( 173 FDA reports)
PALPITATIONS ( 172 FDA reports)
THROMBOCYTOPENIA ( 171 FDA reports)
LOOSE TOOTH ( 169 FDA reports)
OROPHARYNGEAL PAIN ( 169 FDA reports)
TREMOR ( 168 FDA reports)
DYSGEUSIA ( 167 FDA reports)
HYPOPHAGIA ( 162 FDA reports)
AMNESIA ( 161 FDA reports)
JOINT STIFFNESS ( 160 FDA reports)
DIABETES MELLITUS ( 159 FDA reports)
TOOTH ABSCESS ( 158 FDA reports)
BONE DEBRIDEMENT ( 156 FDA reports)
GASTRITIS ( 154 FDA reports)
OEDEMA ( 153 FDA reports)
PULMONARY EMBOLISM ( 153 FDA reports)
DRUG INEFFECTIVE ( 152 FDA reports)
PANCYTOPENIA ( 151 FDA reports)
PHYSICAL DISABILITY ( 151 FDA reports)
TACHYCARDIA ( 151 FDA reports)
TRIGGER FINGER ( 151 FDA reports)
PERIODONTITIS ( 150 FDA reports)
THROMBOSIS ( 150 FDA reports)
VERTIGO ( 150 FDA reports)
HIP FRACTURE ( 149 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 144 FDA reports)
ASTHMA ( 143 FDA reports)
CARDIOMEGALY ( 143 FDA reports)
CONTUSION ( 143 FDA reports)
DEBRIDEMENT ( 143 FDA reports)
HYPERHIDROSIS ( 143 FDA reports)
JAW DISORDER ( 143 FDA reports)
RENAL FAILURE ACUTE ( 143 FDA reports)
GINGIVAL PAIN ( 142 FDA reports)
OESOPHAGITIS ( 142 FDA reports)
STOMATITIS ( 141 FDA reports)
ATRIAL FIBRILLATION ( 140 FDA reports)
SCAR ( 140 FDA reports)
GINGIVITIS ( 138 FDA reports)
MYOCARDIAL INFARCTION ( 138 FDA reports)
FOOT FRACTURE ( 136 FDA reports)
ABSCESS JAW ( 135 FDA reports)
MOOD SWINGS ( 134 FDA reports)
RENAL CYST ( 133 FDA reports)
VISUAL IMPAIRMENT ( 133 FDA reports)
OSTEOSCLEROSIS ( 132 FDA reports)
TENDONITIS ( 131 FDA reports)
SINUS DISORDER ( 130 FDA reports)
BREAST CANCER METASTATIC ( 128 FDA reports)
EAR PAIN ( 128 FDA reports)
PLATELET COUNT DECREASED ( 128 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 127 FDA reports)
ORAL DISORDER ( 126 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 126 FDA reports)
COLITIS ( 124 FDA reports)
DRY EYE ( 124 FDA reports)
DECREASED INTEREST ( 123 FDA reports)
NEUTROPENIA ( 123 FDA reports)
LUNG INFILTRATION ( 122 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 121 FDA reports)
FACIAL PAIN ( 121 FDA reports)
NEURALGIA ( 121 FDA reports)
RECTAL HAEMORRHAGE ( 121 FDA reports)
SOMNOLENCE ( 121 FDA reports)
VAGINAL HAEMORRHAGE ( 121 FDA reports)
CHOLELITHIASIS ( 120 FDA reports)
GINGIVAL SWELLING ( 120 FDA reports)
MIGRAINE ( 120 FDA reports)
TOOTH FRACTURE ( 120 FDA reports)
ABDOMINAL DISTENSION ( 119 FDA reports)
ENDODONTIC PROCEDURE ( 119 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 119 FDA reports)
OSTEITIS ( 119 FDA reports)
ASCITES ( 118 FDA reports)
ACTINOMYCOSIS ( 117 FDA reports)
NEOPLASM PROGRESSION ( 117 FDA reports)
SYNOVIAL CYST ( 117 FDA reports)
COMPRESSION FRACTURE ( 116 FDA reports)
JOINT EFFUSION ( 116 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 116 FDA reports)
ABDOMINAL DISCOMFORT ( 115 FDA reports)
CEREBROVASCULAR ACCIDENT ( 115 FDA reports)
CHILLS ( 115 FDA reports)
HERPES ZOSTER ( 115 FDA reports)
HYPOTENSION ( 115 FDA reports)
MASS ( 115 FDA reports)
PATHOLOGICAL FRACTURE ( 114 FDA reports)
GINGIVAL BLEEDING ( 113 FDA reports)
ORAL DISCOMFORT ( 112 FDA reports)
SEPSIS ( 111 FDA reports)
SPINAL COLUMN STENOSIS ( 111 FDA reports)
EPISTAXIS ( 110 FDA reports)
URTICARIA ( 110 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 109 FDA reports)
DISEASE PROGRESSION ( 109 FDA reports)
GINGIVAL DISORDER ( 109 FDA reports)
ADVERSE DRUG REACTION ( 108 FDA reports)
DRUG INTERACTION ( 108 FDA reports)
DYSPHONIA ( 108 FDA reports)
EYE PAIN ( 108 FDA reports)
ROTATOR CUFF SYNDROME ( 108 FDA reports)
DIVERTICULUM INTESTINAL ( 107 FDA reports)
INTERSTITIAL LUNG DISEASE ( 106 FDA reports)
DRY SKIN ( 105 FDA reports)
EXPOSED BONE IN JAW ( 105 FDA reports)
MOOD ALTERED ( 105 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 105 FDA reports)
DIVERTICULUM ( 104 FDA reports)
HAEMOGLOBIN DECREASED ( 104 FDA reports)
NASOPHARYNGITIS ( 104 FDA reports)
PERIODONTAL DISEASE ( 104 FDA reports)
CORONARY ARTERY DISEASE ( 103 FDA reports)
GINGIVAL INFECTION ( 103 FDA reports)
BLOOD CREATININE INCREASED ( 102 FDA reports)
STAPHYLOCOCCAL INFECTION ( 102 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 101 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 101 FDA reports)
JAW OPERATION ( 101 FDA reports)
TOOTH INFECTION ( 101 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 101 FDA reports)
CYST ( 100 FDA reports)
LUNG DISORDER ( 100 FDA reports)
VULVOVAGINAL DRYNESS ( 100 FDA reports)
ABSCESS ( 99 FDA reports)
CHRONIC SINUSITIS ( 98 FDA reports)
HAEMORRHAGE ( 97 FDA reports)
BURNING SENSATION ( 96 FDA reports)
JAW FRACTURE ( 96 FDA reports)
SUICIDAL IDEATION ( 96 FDA reports)
MENTAL STATUS CHANGES ( 95 FDA reports)
NEPHROLITHIASIS ( 95 FDA reports)
ORAL CANDIDIASIS ( 95 FDA reports)
PLEURAL FIBROSIS ( 95 FDA reports)
RADIOTHERAPY ( 94 FDA reports)
BALANCE DISORDER ( 93 FDA reports)
FIBROMYALGIA ( 93 FDA reports)
SEQUESTRECTOMY ( 93 FDA reports)
SLEEP DISORDER ( 93 FDA reports)
FEMUR FRACTURE ( 92 FDA reports)
HEPATIC ENZYME INCREASED ( 92 FDA reports)
DYSURIA ( 91 FDA reports)
WALKING AID USER ( 91 FDA reports)
DIPLOPIA ( 90 FDA reports)
FRACTURE ( 90 FDA reports)
ORAL CAVITY FISTULA ( 90 FDA reports)
RENAL FAILURE CHRONIC ( 90 FDA reports)
OVARIAN CYST ( 89 FDA reports)
RADICULOPATHY ( 89 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 88 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 87 FDA reports)
HYPOAESTHESIA ORAL ( 87 FDA reports)
RESORPTION BONE INCREASED ( 87 FDA reports)
ANKLE FRACTURE ( 86 FDA reports)
GLAUCOMA ( 86 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 86 FDA reports)
HEART RATE INCREASED ( 85 FDA reports)
ARTERIOSCLEROSIS ( 84 FDA reports)
ORAL SURGERY ( 84 FDA reports)
PNEUMOTHORAX ( 84 FDA reports)
SLEEP APNOEA SYNDROME ( 84 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 83 FDA reports)
HEPATIC CYST ( 83 FDA reports)
MENISCUS LESION ( 83 FDA reports)
MOBILITY DECREASED ( 83 FDA reports)
RHEUMATOID ARTHRITIS ( 83 FDA reports)
TENDERNESS ( 83 FDA reports)
WHEEZING ( 83 FDA reports)
DENTURE WEARER ( 82 FDA reports)
EMPHYSEMA ( 82 FDA reports)
ADVERSE EVENT ( 81 FDA reports)
FLATULENCE ( 81 FDA reports)
ONYCHOMYCOSIS ( 81 FDA reports)
CONDITION AGGRAVATED ( 80 FDA reports)
DENTAL OPERATION ( 80 FDA reports)
DISCOMFORT ( 80 FDA reports)
HAEMATOCHEZIA ( 80 FDA reports)
HYPONATRAEMIA ( 80 FDA reports)
HYPOTHYROIDISM ( 80 FDA reports)
TINNITUS ( 80 FDA reports)
DEVICE RELATED INFECTION ( 79 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 79 FDA reports)
LUNG NEOPLASM MALIGNANT ( 79 FDA reports)
MACULAR DEGENERATION ( 79 FDA reports)
ORAL INFECTION ( 79 FDA reports)
TRISMUS ( 79 FDA reports)
UTERINE LEIOMYOMA ( 79 FDA reports)
LOSS OF CONSCIOUSNESS ( 78 FDA reports)
MASTICATION DISORDER ( 78 FDA reports)
OSTEOLYSIS ( 77 FDA reports)
PULMONARY FIBROSIS ( 77 FDA reports)
BASAL CELL CARCINOMA ( 76 FDA reports)
CERVICAL SPINAL STENOSIS ( 76 FDA reports)
HYDRONEPHROSIS ( 76 FDA reports)
LUMBAR SPINAL STENOSIS ( 76 FDA reports)
ROAD TRAFFIC ACCIDENT ( 76 FDA reports)
SKIN LESION ( 76 FDA reports)
CARDIAC DISORDER ( 75 FDA reports)
DYSPNOEA EXERTIONAL ( 75 FDA reports)
MASTECTOMY ( 75 FDA reports)
SPONDYLOLISTHESIS ( 75 FDA reports)
CONVULSION ( 74 FDA reports)
IRON DEFICIENCY ANAEMIA ( 74 FDA reports)
OPEN WOUND ( 73 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 73 FDA reports)
RESPIRATORY FAILURE ( 73 FDA reports)
RHINORRHOEA ( 73 FDA reports)
URINARY INCONTINENCE ( 73 FDA reports)
VAGINAL INFECTION ( 73 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 72 FDA reports)
VISUAL ACUITY REDUCED ( 72 FDA reports)
CHEST DISCOMFORT ( 71 FDA reports)
POLLAKIURIA ( 71 FDA reports)
SKIN DISORDER ( 71 FDA reports)
DYSARTHRIA ( 70 FDA reports)
BONE MARROW FAILURE ( 69 FDA reports)
CARDIAC MURMUR ( 69 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 69 FDA reports)
FACE OEDEMA ( 69 FDA reports)
MUCOSAL INFLAMMATION ( 69 FDA reports)
SPINAL COMPRESSION FRACTURE ( 69 FDA reports)
AGRANULOCYTOSIS ( 68 FDA reports)
HAIR GROWTH ABNORMAL ( 68 FDA reports)
VITREOUS FLOATERS ( 68 FDA reports)
DERMATITIS CONTACT ( 67 FDA reports)
DYSKINESIA ( 67 FDA reports)
EATING DISORDER ( 67 FDA reports)
FOOT DEFORMITY ( 67 FDA reports)
PROTHROMBIN TIME PROLONGED ( 67 FDA reports)
WOUND ( 67 FDA reports)
ABSCESS DRAINAGE ( 66 FDA reports)
BACTERIAL INFECTION ( 66 FDA reports)
DEAFNESS ( 66 FDA reports)
SKIN ULCER ( 66 FDA reports)
WOUND DRAINAGE ( 66 FDA reports)
BREAST PAIN ( 65 FDA reports)
CERVICAL DYSPLASIA ( 65 FDA reports)
DIVERTICULITIS ( 65 FDA reports)
HALLUCINATION ( 65 FDA reports)
KYPHOSIS ( 65 FDA reports)
NAIL DISORDER ( 65 FDA reports)
NASAL CONGESTION ( 65 FDA reports)
ABASIA ( 64 FDA reports)
ANGINA PECTORIS ( 64 FDA reports)
ARRHYTHMIA ( 64 FDA reports)
ECZEMA ( 64 FDA reports)
SPINAL DISORDER ( 64 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 63 FDA reports)
CYSTITIS ( 63 FDA reports)
INFLUENZA LIKE ILLNESS ( 63 FDA reports)
METASTASES TO LYMPH NODES ( 63 FDA reports)
STRESS ( 63 FDA reports)
BREAST MASS ( 62 FDA reports)
CARDIAC FAILURE ( 62 FDA reports)
HYPOGLYCAEMIA ( 62 FDA reports)
MENOPAUSE ( 62 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 62 FDA reports)
DRUG INTOLERANCE ( 61 FDA reports)
PRODUCTIVE COUGH ( 61 FDA reports)
PULMONARY OEDEMA ( 61 FDA reports)
SPINAL FRACTURE ( 61 FDA reports)
EYE DISORDER ( 60 FDA reports)
HEPATIC LESION ( 60 FDA reports)
UPPER LIMB FRACTURE ( 60 FDA reports)
URINARY RETENTION ( 60 FDA reports)
WRIST FRACTURE ( 60 FDA reports)
HAEMATURIA ( 59 FDA reports)
MUSCLE STRAIN ( 59 FDA reports)
PULMONARY HYPERTENSION ( 59 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 59 FDA reports)
BONE NEOPLASM MALIGNANT ( 58 FDA reports)
BONE SCAN ABNORMAL ( 58 FDA reports)
DERMATITIS ( 58 FDA reports)
GASTRIC ULCER ( 58 FDA reports)
HEPATIC FAILURE ( 58 FDA reports)
HYPERCALCAEMIA ( 58 FDA reports)
INGROWING NAIL ( 58 FDA reports)
LIFE EXPECTANCY SHORTENED ( 58 FDA reports)
TUMOUR MARKER INCREASED ( 58 FDA reports)
WOUND DEBRIDEMENT ( 58 FDA reports)
AORTIC VALVE INCOMPETENCE ( 57 FDA reports)
EJECTION FRACTION DECREASED ( 57 FDA reports)
LACRIMATION INCREASED ( 57 FDA reports)
LEUKOPENIA ( 57 FDA reports)
LIVER DISORDER ( 57 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 57 FDA reports)
AGITATION ( 56 FDA reports)
ASPIRATION PLEURAL CAVITY ( 56 FDA reports)
INFLUENZA ( 56 FDA reports)
SEBORRHOEIC KERATOSIS ( 56 FDA reports)
VIITH NERVE PARALYSIS ( 56 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 55 FDA reports)
CONJUNCTIVITIS ( 55 FDA reports)
HORDEOLUM ( 55 FDA reports)
HYPOXIA ( 55 FDA reports)
LEUKOCYTOSIS ( 55 FDA reports)
MYELODYSPLASTIC SYNDROME ( 55 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 55 FDA reports)
RENAL IMPAIRMENT ( 55 FDA reports)
WHEELCHAIR USER ( 55 FDA reports)
CARDIAC ARREST ( 54 FDA reports)
CRYING ( 54 FDA reports)
GALLBLADDER DISORDER ( 54 FDA reports)
GASTROINTESTINAL DISORDER ( 54 FDA reports)
JOINT INJURY ( 54 FDA reports)
NERVOUSNESS ( 54 FDA reports)
OTITIS MEDIA ( 54 FDA reports)
TENDON DISORDER ( 54 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 54 FDA reports)
DEPRESSED MOOD ( 53 FDA reports)
OSTEOMYELITIS CHRONIC ( 53 FDA reports)
THROAT IRRITATION ( 53 FDA reports)
THYROID NEOPLASM ( 53 FDA reports)
ULCER ( 53 FDA reports)
NEURITIS ( 52 FDA reports)
OFF LABEL USE ( 52 FDA reports)
RASH ERYTHEMATOUS ( 52 FDA reports)
SPEECH DISORDER ( 52 FDA reports)
BREAST CANCER FEMALE ( 51 FDA reports)
HEART RATE IRREGULAR ( 51 FDA reports)
HUMERUS FRACTURE ( 51 FDA reports)
HYPERGLYCAEMIA ( 51 FDA reports)
HYPERSENSITIVITY ( 51 FDA reports)
IRRITABLE BOWEL SYNDROME ( 51 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 51 FDA reports)
OBESITY ( 51 FDA reports)
BLOOD URINE PRESENT ( 50 FDA reports)
HEAD INJURY ( 50 FDA reports)
LACERATION ( 50 FDA reports)
LUMBAR RADICULOPATHY ( 50 FDA reports)
METASTATIC NEOPLASM ( 50 FDA reports)
BLOOD BILIRUBIN INCREASED ( 49 FDA reports)
CERVIX CARCINOMA ( 49 FDA reports)
FLUID RETENTION ( 49 FDA reports)
GROIN PAIN ( 49 FDA reports)
JOINT DISLOCATION ( 49 FDA reports)
LARYNGITIS ( 49 FDA reports)
LIMB INJURY ( 49 FDA reports)
REFLUX OESOPHAGITIS ( 49 FDA reports)
RHINITIS ( 49 FDA reports)
VENOUS INSUFFICIENCY ( 49 FDA reports)
BODY HEIGHT DECREASED ( 48 FDA reports)
BREAST CALCIFICATIONS ( 48 FDA reports)
METASTASIS ( 48 FDA reports)
OVARIAN CANCER ( 48 FDA reports)
OVERDOSE ( 48 FDA reports)
RADICULAR PAIN ( 48 FDA reports)
SCIATICA ( 48 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 47 FDA reports)
ADRENAL MASS ( 47 FDA reports)
BONE EROSION ( 47 FDA reports)
DRUG HYPERSENSITIVITY ( 47 FDA reports)
HAND FRACTURE ( 47 FDA reports)
MICTURITION URGENCY ( 47 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 47 FDA reports)
BONE LOSS ( 46 FDA reports)
BONE OPERATION ( 46 FDA reports)
HIP ARTHROPLASTY ( 46 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 46 FDA reports)
IRRITABILITY ( 46 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 46 FDA reports)
LETHARGY ( 46 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 46 FDA reports)
ONYCHOCLASIS ( 46 FDA reports)
PARAESTHESIA ORAL ( 46 FDA reports)
PERICARDIAL EFFUSION ( 46 FDA reports)
RADIATION ASSOCIATED PAIN ( 46 FDA reports)
TOOTH DEPOSIT ( 46 FDA reports)
UROSEPSIS ( 46 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 45 FDA reports)
DISORIENTATION ( 45 FDA reports)
HAEMANGIOMA ( 45 FDA reports)
HEMIPLEGIA ( 45 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 45 FDA reports)
KNEE ARTHROPLASTY ( 45 FDA reports)
ORAL DISCHARGE ( 45 FDA reports)
RENAL PAIN ( 45 FDA reports)
VISUAL DISTURBANCE ( 45 FDA reports)
ANGER ( 44 FDA reports)
BLOOD UREA INCREASED ( 44 FDA reports)
BONE FRAGMENTATION ( 44 FDA reports)
BREATH ODOUR ( 44 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 44 FDA reports)
FEELING HOT ( 44 FDA reports)
FLUSHING ( 44 FDA reports)
HYPERKERATOSIS ( 44 FDA reports)
LEFT ATRIAL DILATATION ( 44 FDA reports)
PANCREATITIS ( 44 FDA reports)
PROTEINURIA ( 44 FDA reports)
UTERINE HAEMORRHAGE ( 44 FDA reports)
BLOOD GLUCOSE DECREASED ( 43 FDA reports)
DISTURBANCE IN ATTENTION ( 43 FDA reports)
DYSTONIA ( 43 FDA reports)
GINGIVAL OEDEMA ( 43 FDA reports)
HAEMATOCRIT DECREASED ( 43 FDA reports)
HAEMOPTYSIS ( 43 FDA reports)
HEPATOMEGALY ( 43 FDA reports)
JOINT SPRAIN ( 43 FDA reports)
RECURRENT CANCER ( 43 FDA reports)
SINUS BRADYCARDIA ( 43 FDA reports)
TONGUE ULCERATION ( 43 FDA reports)
DERMAL CYST ( 42 FDA reports)
DYSSTASIA ( 42 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 42 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 42 FDA reports)
MEDICATION ERROR ( 42 FDA reports)
PANCREATITIS ACUTE ( 42 FDA reports)
PELVIC PAIN ( 42 FDA reports)
PULMONARY CONGESTION ( 42 FDA reports)
SEASONAL ALLERGY ( 42 FDA reports)
SKIN EXFOLIATION ( 42 FDA reports)
ANOREXIA ( 41 FDA reports)
FLANK PAIN ( 41 FDA reports)
IMPLANT SITE INFECTION ( 41 FDA reports)
MENTAL DISORDER ( 41 FDA reports)
PLANTAR FASCIITIS ( 41 FDA reports)
PROCEDURAL PAIN ( 41 FDA reports)
RESPIRATORY DEPRESSION ( 41 FDA reports)
RETINAL HAEMORRHAGE ( 41 FDA reports)
RHINITIS ALLERGIC ( 41 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 41 FDA reports)
SEDATION ( 41 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 40 FDA reports)
COGNITIVE DISORDER ( 40 FDA reports)
DENTAL PLAQUE ( 40 FDA reports)
DISEASE RECURRENCE ( 40 FDA reports)
FEELING COLD ( 40 FDA reports)
MOVEMENT DISORDER ( 40 FDA reports)
MULTI-ORGAN FAILURE ( 40 FDA reports)
SINUS HEADACHE ( 40 FDA reports)
VARICOSE VEIN ( 40 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 39 FDA reports)
ASPIRATION ( 39 FDA reports)
BLISTER ( 39 FDA reports)
BLOOD CALCIUM DECREASED ( 39 FDA reports)
BLOOD POTASSIUM DECREASED ( 39 FDA reports)
COLONIC POLYP ( 39 FDA reports)
GRIP STRENGTH DECREASED ( 39 FDA reports)
INTENTIONAL DRUG MISUSE ( 39 FDA reports)
JAUNDICE ( 39 FDA reports)
LYMPHOMA ( 39 FDA reports)
ODYNOPHAGIA ( 39 FDA reports)
UTERINE CANCER ( 39 FDA reports)
CANDIDIASIS ( 38 FDA reports)
DYSLIPIDAEMIA ( 38 FDA reports)
GOITRE ( 38 FDA reports)
HAIR TEXTURE ABNORMAL ( 38 FDA reports)
HYSTERECTOMY ( 38 FDA reports)
LOCALISED INFECTION ( 38 FDA reports)
NEOPLASM ( 38 FDA reports)
QUALITY OF LIFE DECREASED ( 38 FDA reports)
CHROMATURIA ( 37 FDA reports)
DECUBITUS ULCER ( 37 FDA reports)
FACIAL BONES FRACTURE ( 37 FDA reports)
MALNUTRITION ( 37 FDA reports)
SKIN LACERATION ( 37 FDA reports)
SPINAL DECOMPRESSION ( 37 FDA reports)
COMA ( 36 FDA reports)
DUODENITIS ( 36 FDA reports)
GINGIVAL RECESSION ( 36 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 36 FDA reports)
RADIUS FRACTURE ( 36 FDA reports)
RASH PRURITIC ( 36 FDA reports)
SINUS CONGESTION ( 36 FDA reports)
WOUND DEHISCENCE ( 36 FDA reports)
X-RAY ABNORMAL ( 36 FDA reports)
ABDOMINAL HERNIA ( 35 FDA reports)
APHASIA ( 35 FDA reports)
ATROPHIC VULVOVAGINITIS ( 35 FDA reports)
BLINDNESS ( 35 FDA reports)
CARDIOMYOPATHY ( 35 FDA reports)
GINGIVAL ULCERATION ( 35 FDA reports)
HYPERKALAEMIA ( 35 FDA reports)
HYPERPLASIA ( 35 FDA reports)
INJECTION SITE PAIN ( 35 FDA reports)
POSTURE ABNORMAL ( 35 FDA reports)
SEROMA ( 35 FDA reports)
SKELETAL INJURY ( 35 FDA reports)
AGEUSIA ( 34 FDA reports)
BRADYCARDIA ( 34 FDA reports)
BREAST CYST ( 34 FDA reports)
BREAST TENDERNESS ( 34 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 34 FDA reports)
CORNEAL DYSTROPHY ( 34 FDA reports)
FIBROSIS ( 34 FDA reports)
HEPATIC CIRRHOSIS ( 34 FDA reports)
HYPOACUSIS ( 34 FDA reports)
LIMB DISCOMFORT ( 34 FDA reports)
MALIGNANT MELANOMA ( 34 FDA reports)
PURULENCE ( 34 FDA reports)
SOFT TISSUE DISORDER ( 34 FDA reports)
STOMACH DISCOMFORT ( 34 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 34 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 34 FDA reports)
ACCIDENTAL OVERDOSE ( 33 FDA reports)
ACTINIC KERATOSIS ( 33 FDA reports)
ANOGENITAL WARTS ( 33 FDA reports)
AZOTAEMIA ( 33 FDA reports)
BLOOD PRESSURE DECREASED ( 33 FDA reports)
DEPRESSIVE SYMPTOM ( 33 FDA reports)
ECCHYMOSIS ( 33 FDA reports)
GOUT ( 33 FDA reports)
HAEMATEMESIS ( 33 FDA reports)
HYPERTONIC BLADDER ( 33 FDA reports)
IMPAIRED WORK ABILITY ( 33 FDA reports)
ISCHAEMIA ( 33 FDA reports)
LABYRINTHITIS ( 33 FDA reports)
LIBIDO DECREASED ( 33 FDA reports)
LIGAMENT SPRAIN ( 33 FDA reports)
MELANOCYTIC NAEVUS ( 33 FDA reports)
MENOPAUSAL SYMPTOMS ( 33 FDA reports)
OSTEORADIONECROSIS ( 33 FDA reports)
SYNOVITIS ( 33 FDA reports)
CALCINOSIS ( 32 FDA reports)
CEREBRAL ISCHAEMIA ( 32 FDA reports)
CHEST WALL OPERATION ( 32 FDA reports)
DEVICE FAILURE ( 32 FDA reports)
EYE HAEMORRHAGE ( 32 FDA reports)
FEBRILE NEUTROPENIA ( 32 FDA reports)
FOREIGN BODY ( 32 FDA reports)
INCORRECT DOSE ADMINISTERED ( 32 FDA reports)
INTERTRIGO ( 32 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 32 FDA reports)
LOCAL SWELLING ( 32 FDA reports)
MAXILLOFACIAL OPERATION ( 32 FDA reports)
MELAENA ( 32 FDA reports)
PELVIC FRACTURE ( 32 FDA reports)
SQUAMOUS CELL CARCINOMA ( 32 FDA reports)
THROMBOPHLEBITIS ( 32 FDA reports)
TYPE 2 DIABETES MELLITUS ( 32 FDA reports)
UTERINE POLYP ( 32 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 31 FDA reports)
BACK DISORDER ( 31 FDA reports)
DELUSION ( 31 FDA reports)
FAECAL INCONTINENCE ( 31 FDA reports)
FUNGAL INFECTION ( 31 FDA reports)
HAEMATOMA ( 31 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 31 FDA reports)
MYOPATHY ( 31 FDA reports)
NEURODERMATITIS ( 31 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 31 FDA reports)
RESPIRATORY DISTRESS ( 31 FDA reports)
RESTLESS LEGS SYNDROME ( 31 FDA reports)
SENSITIVITY OF TEETH ( 31 FDA reports)
SINUS TACHYCARDIA ( 31 FDA reports)
SKIN DISCOLOURATION ( 31 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 30 FDA reports)
BLINDNESS UNILATERAL ( 30 FDA reports)
CEREBRAL HAEMORRHAGE ( 30 FDA reports)
CHOLECYSTITIS ( 30 FDA reports)
EXCORIATION ( 30 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 30 FDA reports)
HEARING IMPAIRED ( 30 FDA reports)
HYPOAESTHESIA FACIAL ( 30 FDA reports)
INCONTINENCE ( 30 FDA reports)
MEDICAL DEVICE REMOVAL ( 30 FDA reports)
METRORRHAGIA ( 30 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 30 FDA reports)
PAPILLOMA ( 30 FDA reports)
POLYARTHRITIS ( 30 FDA reports)
RESTLESSNESS ( 30 FDA reports)
SKIN CANCER ( 30 FDA reports)
TIBIA FRACTURE ( 30 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 29 FDA reports)
ASEPTIC NECROSIS BONE ( 29 FDA reports)
BREAST SWELLING ( 29 FDA reports)
CHEST WALL MASS ( 29 FDA reports)
DYSPLASIA ( 29 FDA reports)
GRANULOMA ( 29 FDA reports)
ILEUS PARALYTIC ( 29 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 29 FDA reports)
PALATAL DISORDER ( 29 FDA reports)
PERIODONTAL INFECTION ( 29 FDA reports)
POOR QUALITY SLEEP ( 29 FDA reports)
SPINAL LAMINECTOMY ( 29 FDA reports)
STREPTOCOCCAL INFECTION ( 29 FDA reports)
TOOTH IMPACTED ( 29 FDA reports)
VITAMIN D DEFICIENCY ( 29 FDA reports)
ABSCESS ORAL ( 28 FDA reports)
BONE SWELLING ( 28 FDA reports)
CYSTOCELE ( 28 FDA reports)
DENTAL CARE ( 28 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 28 FDA reports)
FACIAL PALSY ( 28 FDA reports)
FISTULA REPAIR ( 28 FDA reports)
HYPOPHOSPHATAEMIA ( 28 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 28 FDA reports)
MASS EXCISION ( 28 FDA reports)
NOCTURIA ( 28 FDA reports)
PALLOR ( 28 FDA reports)
POOR PERSONAL HYGIENE ( 28 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 28 FDA reports)
PULMONARY GRANULOMA ( 28 FDA reports)
RESPIRATORY TRACT INFECTION ( 28 FDA reports)
TENOSYNOVITIS ( 28 FDA reports)
TOOTH EROSION ( 28 FDA reports)
ULCERATIVE KERATITIS ( 28 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 28 FDA reports)
WEIGHT LOSS POOR ( 28 FDA reports)
AXILLARY MASS ( 27 FDA reports)
BACTERIAL TEST POSITIVE ( 27 FDA reports)
BLOOD CALCIUM INCREASED ( 27 FDA reports)
CHOLECYSTECTOMY ( 27 FDA reports)
DIASTOLIC DYSFUNCTION ( 27 FDA reports)
EMOTIONAL DISORDER ( 27 FDA reports)
EYE INFECTION ( 27 FDA reports)
FEAR ( 27 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 27 FDA reports)
GINGIVAL ABSCESS ( 27 FDA reports)
HAIR DISORDER ( 27 FDA reports)
HYPERCOAGULATION ( 27 FDA reports)
HYPERSOMNIA ( 27 FDA reports)
ILEUS ( 27 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 27 FDA reports)
KIDNEY INFECTION ( 27 FDA reports)
NERVOUS SYSTEM DISORDER ( 27 FDA reports)
NEUROGENIC BLADDER ( 27 FDA reports)
OESOPHAGEAL ULCER ( 27 FDA reports)
PARKINSON'S DISEASE ( 27 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 27 FDA reports)
TREATMENT NONCOMPLIANCE ( 27 FDA reports)
VISUAL FIELD DEFECT ( 27 FDA reports)
WOUND TREATMENT ( 27 FDA reports)
ANGIOEDEMA ( 26 FDA reports)
AORTIC VALVE STENOSIS ( 26 FDA reports)
APHAGIA ( 26 FDA reports)
ATROPHY ( 26 FDA reports)
BREAST LUMP REMOVAL ( 26 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 26 FDA reports)
CEREBRAL ATROPHY ( 26 FDA reports)
COORDINATION ABNORMAL ( 26 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 26 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 26 FDA reports)
EYE SWELLING ( 26 FDA reports)
LIPOMA ( 26 FDA reports)
LUNG HYPERINFLATION ( 26 FDA reports)
MAJOR DEPRESSION ( 26 FDA reports)
METABOLIC ACIDOSIS ( 26 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 26 FDA reports)
MUSCLE TIGHTNESS ( 26 FDA reports)
OROANTRAL FISTULA ( 26 FDA reports)
PRESYNCOPE ( 26 FDA reports)
RECTAL FISSURE ( 26 FDA reports)
RETINOPATHY ( 26 FDA reports)
SEPTIC SHOCK ( 26 FDA reports)
SKIN REACTION ( 26 FDA reports)
TONGUE INJURY ( 26 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 26 FDA reports)
VIRAL INFECTION ( 26 FDA reports)
WALKING DISABILITY ( 26 FDA reports)
ALVEOLAR OSTEITIS ( 25 FDA reports)
APHONIA ( 25 FDA reports)
DENTAL TREATMENT ( 25 FDA reports)
FACE INJURY ( 25 FDA reports)
FAECES DISCOLOURED ( 25 FDA reports)
GENITAL HERPES ( 25 FDA reports)
HEART VALVE INCOMPETENCE ( 25 FDA reports)
HERNIA ( 25 FDA reports)
HYPOCALCAEMIA ( 25 FDA reports)
INCISIONAL DRAINAGE ( 25 FDA reports)
LIP SWELLING ( 25 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 25 FDA reports)
MENINGITIS ( 25 FDA reports)
MENTAL IMPAIRMENT ( 25 FDA reports)
MOUTH HAEMORRHAGE ( 25 FDA reports)
MYOSITIS ( 25 FDA reports)
NODULE ( 25 FDA reports)
OEDEMA MUCOSAL ( 25 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 25 FDA reports)
PERIODONTAL OPERATION ( 25 FDA reports)
PLEURODESIS ( 25 FDA reports)
POLYNEUROPATHY ( 25 FDA reports)
SACROILIITIS ( 25 FDA reports)
SMEAR CERVIX ABNORMAL ( 25 FDA reports)
STRESS FRACTURE ( 25 FDA reports)
ABDOMINAL PAIN LOWER ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 24 FDA reports)
BILE DUCT STONE ( 24 FDA reports)
BIOPSY ( 24 FDA reports)
EATING DISORDER SYMPTOM ( 24 FDA reports)
ERUCTATION ( 24 FDA reports)
ESSENTIAL HYPERTENSION ( 24 FDA reports)
EYE PRURITUS ( 24 FDA reports)
FACET JOINT SYNDROME ( 24 FDA reports)
METASTASES TO SKIN ( 24 FDA reports)
OEDEMA MOUTH ( 24 FDA reports)
PANIC DISORDER ( 24 FDA reports)
PROCTALGIA ( 24 FDA reports)
PRODUCT QUALITY ISSUE ( 24 FDA reports)
SENSATION OF HEAVINESS ( 24 FDA reports)
SKIN NECROSIS ( 24 FDA reports)
SKIN PAPILLOMA ( 24 FDA reports)
SPINAL CORD COMPRESSION ( 24 FDA reports)
TINEA PEDIS ( 24 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 24 FDA reports)
TRIGEMINAL NEURALGIA ( 24 FDA reports)
VAGINAL DISCHARGE ( 24 FDA reports)
WITHDRAWAL SYNDROME ( 24 FDA reports)
APPENDICITIS ( 23 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 23 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 23 FDA reports)
CEREBRAL INFARCTION ( 23 FDA reports)
ENDOMETRIAL DISORDER ( 23 FDA reports)
EYELID OEDEMA ( 23 FDA reports)
METASTASES TO SPLEEN ( 23 FDA reports)
METASTATIC PAIN ( 23 FDA reports)
MITRAL VALVE PROLAPSE ( 23 FDA reports)
MYOCARDIAL ISCHAEMIA ( 23 FDA reports)
NERVE INJURY ( 23 FDA reports)
OOPHORECTOMY ( 23 FDA reports)
ORTHOSIS USER ( 23 FDA reports)
PHARYNGITIS ( 23 FDA reports)
PLASTIC SURGERY TO THE FACE ( 23 FDA reports)
RADIATION INJURY ( 23 FDA reports)
RASH MACULAR ( 23 FDA reports)
RECTOCELE ( 23 FDA reports)
SKIN ATROPHY ( 23 FDA reports)
SPINAL FUSION SURGERY ( 23 FDA reports)
SPLENOMEGALY ( 23 FDA reports)
SUDDEN DEATH ( 23 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 23 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 23 FDA reports)
ADENOMYOSIS ( 22 FDA reports)
AREFLEXIA ( 22 FDA reports)
BEDRIDDEN ( 22 FDA reports)
BONE GRAFT ( 22 FDA reports)
BONE TRIMMING ( 22 FDA reports)
CHONDROMALACIA ( 22 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 22 FDA reports)
EARLY SATIETY ( 22 FDA reports)
ESCHERICHIA INFECTION ( 22 FDA reports)
GASTROENTERITIS VIRAL ( 22 FDA reports)
GINGIVAL EROSION ( 22 FDA reports)
HAEMANGIOMA OF LIVER ( 22 FDA reports)
HAEMOLYTIC ANAEMIA ( 22 FDA reports)
HEPATITIS ( 22 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 22 FDA reports)
JAUNDICE CHOLESTATIC ( 22 FDA reports)
MELANOSIS COLI ( 22 FDA reports)
METASTASES TO MENINGES ( 22 FDA reports)
NASAL MUCOSAL DISORDER ( 22 FDA reports)
PANIC ATTACK ( 22 FDA reports)
RECTAL ABSCESS ( 22 FDA reports)
WOUND SECRETION ( 22 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 21 FDA reports)
BRUXISM ( 21 FDA reports)
COCCYDYNIA ( 21 FDA reports)
CONNECTIVE TISSUE DISORDER ( 21 FDA reports)
COSTOCHONDRITIS ( 21 FDA reports)
DEAFNESS UNILATERAL ( 21 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 21 FDA reports)
EYELID PTOSIS ( 21 FDA reports)
FOLLICULITIS ( 21 FDA reports)
GASTROENTERITIS ( 21 FDA reports)
HYPOALBUMINAEMIA ( 21 FDA reports)
INCREASED APPETITE ( 21 FDA reports)
LUNG INFECTION ( 21 FDA reports)
LYMPHADENECTOMY ( 21 FDA reports)
METASTASES TO THE MEDIASTINUM ( 21 FDA reports)
MYELOPATHY ( 21 FDA reports)
NECROSIS ( 21 FDA reports)
OCCULT BLOOD POSITIVE ( 21 FDA reports)
OVARIAN MASS ( 21 FDA reports)
PLATELET COUNT INCREASED ( 21 FDA reports)
PROSTHESIS IMPLANTATION ( 21 FDA reports)
SKIN BURNING SENSATION ( 21 FDA reports)
STASIS DERMATITIS ( 21 FDA reports)
STOMATOCYTES PRESENT ( 21 FDA reports)
TENDON INJURY ( 21 FDA reports)
THORACOSTOMY ( 21 FDA reports)
UNRESPONSIVE TO STIMULI ( 21 FDA reports)
ACNE ( 20 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 20 FDA reports)
ASBESTOSIS ( 20 FDA reports)
ATAXIA ( 20 FDA reports)
BLOOD CREATININE DECREASED ( 20 FDA reports)
BONE FORMATION INCREASED ( 20 FDA reports)
CARDIO-RESPIRATORY ARREST ( 20 FDA reports)
COLON CANCER ( 20 FDA reports)
COLONOSCOPY ABNORMAL ( 20 FDA reports)
DENTAL FISTULA ( 20 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 20 FDA reports)
DYSPAREUNIA ( 20 FDA reports)
ENCEPHALOPATHY ( 20 FDA reports)
GLOSSODYNIA ( 20 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 20 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 20 FDA reports)
LIGAMENT RUPTURE ( 20 FDA reports)
LOWER LIMB FRACTURE ( 20 FDA reports)
MIDDLE INSOMNIA ( 20 FDA reports)
MUSCLE TWITCHING ( 20 FDA reports)
NEUROPATHY ( 20 FDA reports)
OCULAR HYPERAEMIA ( 20 FDA reports)
PARANOIA ( 20 FDA reports)
PERONEAL NERVE PALSY ( 20 FDA reports)
PETECHIAE ( 20 FDA reports)
PHOTOPSIA ( 20 FDA reports)
PHYSIOTHERAPY ( 20 FDA reports)
PYURIA ( 20 FDA reports)
RENAL DISORDER ( 20 FDA reports)
URINE ODOUR ABNORMAL ( 20 FDA reports)
VERTEBRAL WEDGING ( 20 FDA reports)
AGGRESSION ( 19 FDA reports)
AORTIC VALVE REPLACEMENT ( 19 FDA reports)
BLINDNESS TRANSIENT ( 19 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 19 FDA reports)
BREAST CANCER IN SITU ( 19 FDA reports)
BREAST RECONSTRUCTION ( 19 FDA reports)
BREATH SOUNDS ABNORMAL ( 19 FDA reports)
BRONCHITIS CHRONIC ( 19 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 19 FDA reports)
CYST ASPIRATION ( 19 FDA reports)
CYSTITIS HAEMORRHAGIC ( 19 FDA reports)
DRY THROAT ( 19 FDA reports)
ENDOCARDITIS ( 19 FDA reports)
EXTERNAL EAR DISORDER ( 19 FDA reports)
FEMORAL NECK FRACTURE ( 19 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 19 FDA reports)
GLOSSITIS ( 19 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 19 FDA reports)
HYPERTHYROIDISM ( 19 FDA reports)
HYPOKINESIA ( 19 FDA reports)
MACROCYTOSIS ( 19 FDA reports)
MEDIASTINAL MASS ( 19 FDA reports)
NERVE BLOCK ( 19 FDA reports)
ONYCHALGIA ( 19 FDA reports)
PERIPHERAL COLDNESS ( 19 FDA reports)
PHOTOSENSITIVITY REACTION ( 19 FDA reports)
PLASTIC SURGERY ( 19 FDA reports)
PULMONARY MASS ( 19 FDA reports)
PYODERMA GANGRENOSUM ( 19 FDA reports)
RADICULAR SYNDROME ( 19 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 19 FDA reports)
SPINAL DEFORMITY ( 19 FDA reports)
TENOSYNOVITIS STENOSANS ( 19 FDA reports)
TOOTH DISCOLOURATION ( 19 FDA reports)
TOOTH INJURY ( 19 FDA reports)
ABNORMAL DREAMS ( 18 FDA reports)
ACUTE CORONARY SYNDROME ( 18 FDA reports)
ADRENAL ADENOMA ( 18 FDA reports)
ADRENAL INSUFFICIENCY ( 18 FDA reports)
ATRIAL FLUTTER ( 18 FDA reports)
BONE ATROPHY ( 18 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 18 FDA reports)
BULLOUS LUNG DISEASE ( 18 FDA reports)
CARDIAC PACEMAKER INSERTION ( 18 FDA reports)
CATHETER PLACEMENT ( 18 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 18 FDA reports)
CHOLESTASIS ( 18 FDA reports)
EPICONDYLITIS ( 18 FDA reports)
ERECTILE DYSFUNCTION ( 18 FDA reports)
EYE IRRITATION ( 18 FDA reports)
GASTRIC DISORDER ( 18 FDA reports)
HYPOVOLAEMIA ( 18 FDA reports)
IRITIS ( 18 FDA reports)
MANDIBULAR PROSTHESIS USER ( 18 FDA reports)
MANIA ( 18 FDA reports)
METAPLASIA ( 18 FDA reports)
PEPTIC ULCER ( 18 FDA reports)
POOR PERIPHERAL CIRCULATION ( 18 FDA reports)
POST-TRAUMATIC PAIN ( 18 FDA reports)
PROSTATOMEGALY ( 18 FDA reports)
RALES ( 18 FDA reports)
SNORING ( 18 FDA reports)
STENT PLACEMENT ( 18 FDA reports)
SWOLLEN TONGUE ( 18 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 18 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 18 FDA reports)
URETERIC OBSTRUCTION ( 18 FDA reports)
URETHRAL STENOSIS ( 18 FDA reports)
VOCAL CORD PARALYSIS ( 18 FDA reports)
ACCIDENT AT WORK ( 17 FDA reports)
ACCOMMODATION DISORDER ( 17 FDA reports)
AORTIC ANEURYSM ( 17 FDA reports)
APLASTIC ANAEMIA ( 17 FDA reports)
BIOPSY BONE ( 17 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 17 FDA reports)
BLOOD SODIUM DECREASED ( 17 FDA reports)
CARDIAC VALVE DISEASE ( 17 FDA reports)
CAROTID BRUIT ( 17 FDA reports)
CATARACT NUCLEAR ( 17 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 17 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 17 FDA reports)
DRUG TOXICITY ( 17 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 17 FDA reports)
FURUNCLE ( 17 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 17 FDA reports)
GRAM STAIN POSITIVE ( 17 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 17 FDA reports)
LICHENOID KERATOSIS ( 17 FDA reports)
MENORRHAGIA ( 17 FDA reports)
METASTASES TO ADRENALS ( 17 FDA reports)
MICROANGIOPATHY ( 17 FDA reports)
MITRAL VALVE CALCIFICATION ( 17 FDA reports)
NEOPLASM RECURRENCE ( 17 FDA reports)
OESTRADIOL INCREASED ( 17 FDA reports)
ORAL INTAKE REDUCED ( 17 FDA reports)
ORTHOSTATIC HYPOTENSION ( 17 FDA reports)
PAIN OF SKIN ( 17 FDA reports)
RADICAL HYSTERECTOMY ( 17 FDA reports)
RENAL ATROPHY ( 17 FDA reports)
SCHAMBERG'S DISEASE ( 17 FDA reports)
SKIN FISSURES ( 17 FDA reports)
SKIN WRINKLING ( 17 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 17 FDA reports)
TENDON RUPTURE ( 17 FDA reports)
ULNAR NEURITIS ( 17 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 17 FDA reports)
URETERAL DISORDER ( 17 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 17 FDA reports)
WOUND HAEMORRHAGE ( 17 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 17 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
AORTIC CALCIFICATION ( 16 FDA reports)
ASTIGMATISM ( 16 FDA reports)
BODY TINEA ( 16 FDA reports)
BREAST INDURATION ( 16 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 16 FDA reports)
CACHEXIA ( 16 FDA reports)
CAROTID BODY TUMOUR ( 16 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 16 FDA reports)
CHEILITIS ( 16 FDA reports)
CONJUNCTIVOCHALASIS ( 16 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 16 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 16 FDA reports)
CYST RUPTURE ( 16 FDA reports)
DELIRIUM ( 16 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 16 FDA reports)
DERMATITIS ATOPIC ( 16 FDA reports)
DIABETIC FOOT ( 16 FDA reports)
DIAPHRAGMATIC HERNIA ( 16 FDA reports)
DRUG DEPENDENCE ( 16 FDA reports)
DYSTHYMIC DISORDER ( 16 FDA reports)
ENTHESOPATHY ( 16 FDA reports)
GASTRIC CANCER ( 16 FDA reports)
GLARE ( 16 FDA reports)
HYPOMANIA ( 16 FDA reports)
IMMUNE SYSTEM DISORDER ( 16 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 16 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 16 FDA reports)
LACTOSE INTOLERANCE ( 16 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 16 FDA reports)
METASTASES TO NASAL SINUSES ( 16 FDA reports)
MUCOSAL EROSION ( 16 FDA reports)
MUSCULOSKELETAL DISORDER ( 16 FDA reports)
OXYGEN SATURATION DECREASED ( 16 FDA reports)
PANCREATIC CALCIFICATION ( 16 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 16 FDA reports)
PERIARTHRITIS ( 16 FDA reports)
PHARYNGEAL ERYTHEMA ( 16 FDA reports)
PHLEBITIS ( 16 FDA reports)
PHOTOPHOBIA ( 16 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 16 FDA reports)
PNEUMONITIS ( 16 FDA reports)
POST PROCEDURAL COMPLICATION ( 16 FDA reports)
RETCHING ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
SENSORY DISTURBANCE ( 16 FDA reports)
SPUTUM PURULENT ( 16 FDA reports)
STOMATITIS NECROTISING ( 16 FDA reports)
THROAT TIGHTNESS ( 16 FDA reports)
THYROID DISORDER ( 16 FDA reports)
TRANSFUSION ( 16 FDA reports)
UMBILICAL HERNIA ( 16 FDA reports)
VASCULAR CALCIFICATION ( 16 FDA reports)
ABNORMAL SENSATION IN EYE ( 15 FDA reports)
ALVEOLOPLASTY ( 15 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 15 FDA reports)
BIOPSY BLADDER ABNORMAL ( 15 FDA reports)
BIOPSY BONE ABNORMAL ( 15 FDA reports)
BIOPSY SKIN ABNORMAL ( 15 FDA reports)
BLADDER NEOPLASM ( 15 FDA reports)
BLOOD POTASSIUM INCREASED ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 15 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 15 FDA reports)
BONE CYST ( 15 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 15 FDA reports)
BUNION ( 15 FDA reports)
CERVICAL CORD COMPRESSION ( 15 FDA reports)
CERVICOBRACHIAL SYNDROME ( 15 FDA reports)
CYSTITIS INTERSTITIAL ( 15 FDA reports)
DENTAL PROSTHESIS USER ( 15 FDA reports)
DENTAL PULP DISORDER ( 15 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 15 FDA reports)
ENTERITIS ( 15 FDA reports)
HOSPITALISATION ( 15 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 15 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 15 FDA reports)
INTERMITTENT CLAUDICATION ( 15 FDA reports)
JOINT CREPITATION ( 15 FDA reports)
LOBAR PNEUMONIA ( 15 FDA reports)
LUNG CONSOLIDATION ( 15 FDA reports)
MICROCYTIC ANAEMIA ( 15 FDA reports)
MITRAL VALVE DISEASE ( 15 FDA reports)
MUSCLE DISORDER ( 15 FDA reports)
NEUTROPHIL COUNT DECREASED ( 15 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 15 FDA reports)
PANCREATIC CYST ( 15 FDA reports)
PANCREATIC NEOPLASM ( 15 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 15 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 15 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 15 FDA reports)
PRURITUS GENITAL ( 15 FDA reports)
RETINAL TEAR ( 15 FDA reports)
SJOGREN'S SYNDROME ( 15 FDA reports)
SKIN HYPERPIGMENTATION ( 15 FDA reports)
SOFT TISSUE INFECTION ( 15 FDA reports)
SPINAL CORPECTOMY ( 15 FDA reports)
SPUTUM DISCOLOURED ( 15 FDA reports)
STEVENS-JOHNSON SYNDROME ( 15 FDA reports)
TEMPERATURE INTOLERANCE ( 15 FDA reports)
TENDON PAIN ( 15 FDA reports)
TIC ( 15 FDA reports)
ANOSMIA ( 14 FDA reports)
AORTIC DISORDER ( 14 FDA reports)
ARTHROSCOPY ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK ( 14 FDA reports)
BARRETT'S OESOPHAGUS ( 14 FDA reports)
BLOOD ALBUMIN DECREASED ( 14 FDA reports)
BODY TEMPERATURE INCREASED ( 14 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 14 FDA reports)
CHEMICAL POISONING ( 14 FDA reports)
CREPITATIONS ( 14 FDA reports)
DEMENTIA ( 14 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 14 FDA reports)
DENTAL IMPLANTATION ( 14 FDA reports)
ESCHERICHIA SEPSIS ( 14 FDA reports)
EYE ABSCESS ( 14 FDA reports)
FAECALOMA ( 14 FDA reports)
FEELING JITTERY ( 14 FDA reports)
FLUID REPLACEMENT ( 14 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 14 FDA reports)
HAEMORRHAGIC STROKE ( 14 FDA reports)
HAND DEFORMITY ( 14 FDA reports)
HEAD DISCOMFORT ( 14 FDA reports)
HYPERTENSIVE CRISIS ( 14 FDA reports)
INFUSION RELATED REACTION ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 14 FDA reports)
LOSS OF LIBIDO ( 14 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 14 FDA reports)
MENINGIOMA ( 14 FDA reports)
METASTASES TO CHEST WALL ( 14 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 14 FDA reports)
OESOPHAGEAL DILATATION ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 14 FDA reports)
ORAL HERPES ( 14 FDA reports)
ORAL TORUS ( 14 FDA reports)
OSTEOSARCOMA METASTATIC ( 14 FDA reports)
PANCREATITIS CHRONIC ( 14 FDA reports)
PYELONEPHRITIS ACUTE ( 14 FDA reports)
SENSORY LOSS ( 14 FDA reports)
SPLENIC GRANULOMA ( 14 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 14 FDA reports)
THYROID CYST ( 14 FDA reports)
ULNA FRACTURE ( 14 FDA reports)
VEIN DISORDER ( 14 FDA reports)
VENTRICULAR TACHYCARDIA ( 14 FDA reports)
ACANTHOMA ( 13 FDA reports)
BLADDER OPERATION ( 13 FDA reports)
BLADDER PROLAPSE ( 13 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 13 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
CARTILAGE INJURY ( 13 FDA reports)
CHANGE OF BOWEL HABIT ( 13 FDA reports)
CYST DRAINAGE ( 13 FDA reports)
DIALYSIS ( 13 FDA reports)
DILATATION ATRIAL ( 13 FDA reports)
DRUG ERUPTION ( 13 FDA reports)
ECONOMIC PROBLEM ( 13 FDA reports)
ELECTROLYTE IMBALANCE ( 13 FDA reports)
ESCHERICHIA BACTERAEMIA ( 13 FDA reports)
GALLBLADDER POLYP ( 13 FDA reports)
GRAFT VERSUS HOST DISEASE ( 13 FDA reports)
HEART RATE DECREASED ( 13 FDA reports)
HYDROCEPHALUS ( 13 FDA reports)
ILIUM FRACTURE ( 13 FDA reports)
IMPAIRED DRIVING ABILITY ( 13 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 13 FDA reports)
INDURATION ( 13 FDA reports)
LACUNAR INFARCTION ( 13 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 13 FDA reports)
MENISCUS REMOVAL ( 13 FDA reports)
METASTASES TO BONE MARROW ( 13 FDA reports)
MONARTHRITIS ( 13 FDA reports)
MOTOR DYSFUNCTION ( 13 FDA reports)
MULTIPLE FRACTURES ( 13 FDA reports)
MULTIPLE MYELOMA ( 13 FDA reports)
NAIL AVULSION ( 13 FDA reports)
NEPHROTIC SYNDROME ( 13 FDA reports)
NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
OESOPHAGEAL MASS ( 13 FDA reports)
ORAL DYSAESTHESIA ( 13 FDA reports)
OSTEITIS DEFORMANS ( 13 FDA reports)
PATELLA FRACTURE ( 13 FDA reports)
PHARYNGEAL OEDEMA ( 13 FDA reports)
PULPITIS DENTAL ( 13 FDA reports)
RASH PAPULAR ( 13 FDA reports)
RENAL CANCER ( 13 FDA reports)
RESPIRATORY DISORDER ( 13 FDA reports)
SALIVARY GLAND MASS ( 13 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 13 FDA reports)
SPLENIC ARTERY ANEURYSM ( 13 FDA reports)
SYSTEMIC SCLEROSIS ( 13 FDA reports)
TOBACCO ABUSE ( 13 FDA reports)
TONGUE DISORDER ( 13 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 13 FDA reports)
VASCULITIS ( 13 FDA reports)
VERTEBROPLASTY ( 13 FDA reports)
VITAMIN D DECREASED ( 13 FDA reports)
VULVAL DISORDER ( 13 FDA reports)
VULVOVAGINAL PRURITUS ( 13 FDA reports)
WOUND INFECTION ( 13 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 12 FDA reports)
ACUTE SINUSITIS ( 12 FDA reports)
ADNEXA UTERI CYST ( 12 FDA reports)
ADNEXA UTERI MASS ( 12 FDA reports)
AFFECT LABILITY ( 12 FDA reports)
AFFECTIVE DISORDER ( 12 FDA reports)
ANGIOPATHY ( 12 FDA reports)
ASTHENOPIA ( 12 FDA reports)
BACTERIAL TEST NEGATIVE ( 12 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 12 FDA reports)
BILIARY COLIC ( 12 FDA reports)
BRONCHOSPASM ( 12 FDA reports)
BURNS THIRD DEGREE ( 12 FDA reports)
CAROTID ARTERY STENOSIS ( 12 FDA reports)
CATARACT OPERATION ( 12 FDA reports)
CHEMOTHERAPY ( 12 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 12 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 12 FDA reports)
CYTOLYTIC HEPATITIS ( 12 FDA reports)
DIABETIC MICROANGIOPATHY ( 12 FDA reports)
DILATATION VENTRICULAR ( 12 FDA reports)
DRUG EFFECT DECREASED ( 12 FDA reports)
DYSPHORIA ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 12 FDA reports)
EROSIVE OESOPHAGITIS ( 12 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 12 FDA reports)
EXERCISE TOLERANCE DECREASED ( 12 FDA reports)
EXTRASYSTOLES ( 12 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 12 FDA reports)
GRANULOCYTOPENIA ( 12 FDA reports)
HEPATIC MASS ( 12 FDA reports)
HEPATIC NEOPLASM ( 12 FDA reports)
HERPES SIMPLEX ( 12 FDA reports)
HYPERAESTHESIA ( 12 FDA reports)
HYPERTRICHOSIS ( 12 FDA reports)
INCISION SITE ERYTHEMA ( 12 FDA reports)
INCISION SITE OEDEMA ( 12 FDA reports)
INTESTINAL POLYP ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
KNEE OPERATION ( 12 FDA reports)
LOCALISED OEDEMA ( 12 FDA reports)
MADAROSIS ( 12 FDA reports)
MALIGNANT MELANOMA IN SITU ( 12 FDA reports)
MENINGEAL NEOPLASM ( 12 FDA reports)
MIGRAINE WITH AURA ( 12 FDA reports)
MULTIPLE INJURIES ( 12 FDA reports)
MUSCLE ATROPHY ( 12 FDA reports)
MUSCLE INJURY ( 12 FDA reports)
MYOPIA ( 12 FDA reports)
NEPHROSCLEROSIS ( 12 FDA reports)
NYSTAGMUS ( 12 FDA reports)
ORAL SOFT TISSUE DISORDER ( 12 FDA reports)
OSTEOMALACIA ( 12 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 12 FDA reports)
PANCOAST'S TUMOUR ( 12 FDA reports)
PAROSMIA ( 12 FDA reports)
PIGMENTATION DISORDER ( 12 FDA reports)
PRURITUS GENERALISED ( 12 FDA reports)
PURPURA ( 12 FDA reports)
RED BLOOD CELLS URINE ( 12 FDA reports)
RENAL ARTERY STENOSIS ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
ROSACEA ( 12 FDA reports)
SALIVARY GLAND CALCULUS ( 12 FDA reports)
SHOCK ( 12 FDA reports)
SKIN HAEMORRHAGE ( 12 FDA reports)
SKIN NODULE ( 12 FDA reports)
SUICIDE ATTEMPT ( 12 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 12 FDA reports)
TEMPORAL ARTERITIS ( 12 FDA reports)
TEMPORAL LOBE EPILEPSY ( 12 FDA reports)
TINEA CRURIS ( 12 FDA reports)
TRANSAMINASES INCREASED ( 12 FDA reports)
UNEVALUABLE EVENT ( 12 FDA reports)
URINE ANALYSIS ( 12 FDA reports)
VENOUS OCCLUSION ( 12 FDA reports)
VERTEBRAL COLUMN MASS ( 12 FDA reports)
VITREOUS DETACHMENT ( 12 FDA reports)
VULVOVAGINAL DISCOMFORT ( 12 FDA reports)
WHITE BLOOD CELL COUNT ( 12 FDA reports)
ABSCESS NECK ( 11 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
ADRENAL DISORDER ( 11 FDA reports)
AMENORRHOEA ( 11 FDA reports)
AORTIC VALVE DISEASE ( 11 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 11 FDA reports)
BLOOD OESTROGEN INCREASED ( 11 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 11 FDA reports)
BLOOD URIC ACID INCREASED ( 11 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 11 FDA reports)
BRAIN NEOPLASM ( 11 FDA reports)
BREAST ABSCESS ( 11 FDA reports)
CERUMEN IMPACTION ( 11 FDA reports)
CHROMATOPSIA ( 11 FDA reports)
COLITIS ISCHAEMIC ( 11 FDA reports)
COMPUTERISED TOMOGRAM ( 11 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 11 FDA reports)
EAR DISORDER ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 11 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 11 FDA reports)
ENDOMETRIOSIS ( 11 FDA reports)
ERYSIPELAS ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 11 FDA reports)
GENERALISED OEDEMA ( 11 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
HEMIPARESIS ( 11 FDA reports)
HYPERPARATHYROIDISM ( 11 FDA reports)
INTESTINAL ISCHAEMIA ( 11 FDA reports)
INTESTINAL RESECTION ( 11 FDA reports)
JOINT ARTHROPLASTY ( 11 FDA reports)
LESION EXCISION ( 11 FDA reports)
LEUKAEMIA ( 11 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
LIPASE INCREASED ( 11 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 11 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 11 FDA reports)
NASAL SEPTUM DEVIATION ( 11 FDA reports)
NASAL SINUS CANCER ( 11 FDA reports)
NECK MASS ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
NIGHTMARE ( 11 FDA reports)
OESOPHAGEAL DISORDER ( 11 FDA reports)
OPEN REDUCTION OF FRACTURE ( 11 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 11 FDA reports)
OSTEOSYNTHESIS ( 11 FDA reports)
PEMPHIGOID ( 11 FDA reports)
PERICARDITIS CONSTRICTIVE ( 11 FDA reports)
POLYP ( 11 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 11 FDA reports)
PROCTITIS ( 11 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 11 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 11 FDA reports)
PULMONARY THROMBOSIS ( 11 FDA reports)
RADICULITIS ( 11 FDA reports)
RENAL TUBULAR ACIDOSIS ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
SALPINGO-OOPHORECTOMY ( 11 FDA reports)
SCRATCH ( 11 FDA reports)
SINUS POLYP ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SKIN INDURATION ( 11 FDA reports)
SKIN IRRITATION ( 11 FDA reports)
SOMNAMBULISM ( 11 FDA reports)
SPLENIC CYST ( 11 FDA reports)
STRESS URINARY INCONTINENCE ( 11 FDA reports)
THERAPEUTIC PROCEDURE ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
THYROID CANCER ( 11 FDA reports)
TOOTH RESORPTION ( 11 FDA reports)
TOXIC SKIN ERUPTION ( 11 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 11 FDA reports)
URINARY TRACT PAIN ( 11 FDA reports)
UTERINE DISORDER ( 11 FDA reports)
VASODILATATION ( 11 FDA reports)
VENTRICULAR FIBRILLATION ( 11 FDA reports)
VENTRICULAR HYPOKINESIA ( 11 FDA reports)
ANAL HAEMORRHAGE ( 10 FDA reports)
ANGIONEUROTIC OEDEMA ( 10 FDA reports)
AUTONOMIC NEUROPATHY ( 10 FDA reports)
BIPOLAR I DISORDER ( 10 FDA reports)
BLEPHARITIS ( 10 FDA reports)
BLOOD PRESSURE ABNORMAL ( 10 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 10 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 10 FDA reports)
BONE FISTULA ( 10 FDA reports)
BONE MARROW OEDEMA ( 10 FDA reports)
BREAST DISORDER ( 10 FDA reports)
BURNS SECOND DEGREE ( 10 FDA reports)
CATHETER REMOVAL ( 10 FDA reports)
CATHETER SITE HAEMATOMA ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CERVICAL POLYP ( 10 FDA reports)
COLON ADENOMA ( 10 FDA reports)
CONJUNCTIVAL PALLOR ( 10 FDA reports)
CYANOSIS ( 10 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 10 FDA reports)
DENTAL DISCOMFORT ( 10 FDA reports)
DEVICE BREAKAGE ( 10 FDA reports)
DRUG ABUSE ( 10 FDA reports)
DRUG ADMINISTRATION ERROR ( 10 FDA reports)
DUODENAL ULCER ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
ENDOMETRIAL CANCER ( 10 FDA reports)
FLUID OVERLOAD ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
HEPATITIS ACUTE ( 10 FDA reports)
HEPATITIS C ( 10 FDA reports)
HEPATITIS TOXIC ( 10 FDA reports)
HIP SURGERY ( 10 FDA reports)
HYDROPNEUMOTHORAX ( 10 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 10 FDA reports)
INTRAOCULAR MELANOMA ( 10 FDA reports)
JAW LESION EXCISION ( 10 FDA reports)
JOINT LOCK ( 10 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
LIGAMENT DISORDER ( 10 FDA reports)
LIGAMENT INJURY ( 10 FDA reports)
MACULE ( 10 FDA reports)
MALOCCLUSION ( 10 FDA reports)
METASTASES TO MOUTH ( 10 FDA reports)
METASTASES TO SOFT TISSUE ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MULTIPLE ALLERGIES ( 10 FDA reports)
NO ADVERSE EVENT ( 10 FDA reports)
OESOPHAGEAL ACHALASIA ( 10 FDA reports)
OPTIC NEUROPATHY ( 10 FDA reports)
ORTHOPNOEA ( 10 FDA reports)
OSTECTOMY ( 10 FDA reports)
PARALYSIS ( 10 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 10 FDA reports)
POOR DENTAL CONDITION ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 10 FDA reports)
PSORIASIS ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 10 FDA reports)
RETINAL DETACHMENT ( 10 FDA reports)
RETINAL SCAR ( 10 FDA reports)
ROTATOR CUFF REPAIR ( 10 FDA reports)
SECRETION DISCHARGE ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SNEEZING ( 10 FDA reports)
SPLENIC LESION ( 10 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 10 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
TACHYARRHYTHMIA ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
TUMOUR INVASION ( 10 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VITAMIN B12 DEFICIENCY ( 10 FDA reports)
VOCAL CORD THICKENING ( 10 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 9 FDA reports)
ADENOCARCINOMA ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
ANORECTAL DISCOMFORT ( 9 FDA reports)
APPETITE DISORDER ( 9 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
ATRIAL TACHYCARDIA ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BACTERIAL DISEASE CARRIER ( 9 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
BENIGN COLONIC NEOPLASM ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
BREAST CANCER STAGE II ( 9 FDA reports)
BREAST DISCOMFORT ( 9 FDA reports)
BREAST OPERATION ( 9 FDA reports)
CANCER PAIN ( 9 FDA reports)
CARDIOTOXICITY ( 9 FDA reports)
CATHETER RELATED COMPLICATION ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
CRANIAL NERVE DISORDER ( 9 FDA reports)
CROHN'S DISEASE ( 9 FDA reports)
CSF TEST ABNORMAL ( 9 FDA reports)
DUODENAL POLYP ( 9 FDA reports)
ENTEROCUTANEOUS FISTULA ( 9 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 9 FDA reports)
EYE DISCHARGE ( 9 FDA reports)
FAILURE TO THRIVE ( 9 FDA reports)
FIBROUS HISTIOCYTOMA ( 9 FDA reports)
FISTULA DISCHARGE ( 9 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 9 FDA reports)
GASTROENTERITIS RADIATION ( 9 FDA reports)
GENITAL DISCHARGE ( 9 FDA reports)
GENITAL HAEMORRHAGE ( 9 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 9 FDA reports)
GLOMERULOSCLEROSIS ( 9 FDA reports)
GRAFT COMPLICATION ( 9 FDA reports)
HAEMORRHOID OPERATION ( 9 FDA reports)
HISTOPLASMOSIS ( 9 FDA reports)
HORNER'S SYNDROME ( 9 FDA reports)
HYPOVENTILATION ( 9 FDA reports)
ILEITIS ( 9 FDA reports)
INJECTION SITE HAEMATOMA ( 9 FDA reports)
INTRAOCULAR LENS IMPLANT ( 9 FDA reports)
LARGE INTESTINAL ULCER ( 9 FDA reports)
LYMPHADENITIS ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MENSTRUAL DISORDER ( 9 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
METASTASES TO PERITONEUM ( 9 FDA reports)
MUCOSAL DRYNESS ( 9 FDA reports)
NAIL OPERATION ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
ORGANISING PNEUMONIA ( 9 FDA reports)
OSTEOMYELITIS DRAINAGE ( 9 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
PERSONALITY CHANGE ( 9 FDA reports)
POLYPECTOMY ( 9 FDA reports)
PORTAL VEIN THROMBOSIS ( 9 FDA reports)
PROSTATE CANCER METASTATIC ( 9 FDA reports)
PROSTATE CANCER RECURRENT ( 9 FDA reports)
PUNCTATE KERATITIS ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
PYELONEPHRITIS ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RESPIRATORY RATE INCREASED ( 9 FDA reports)
RETINAL VEIN OCCLUSION ( 9 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 9 FDA reports)
SIGMOIDITIS ( 9 FDA reports)
SLEEP TERROR ( 9 FDA reports)
SPONDYLITIS ( 9 FDA reports)
TEETH BRITTLE ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
THIRST ( 9 FDA reports)
TONGUE PARALYSIS ( 9 FDA reports)
TROPONIN I INCREASED ( 9 FDA reports)
VAGINAL CANCER ( 9 FDA reports)
VAGINAL PAIN ( 9 FDA reports)
VENOUS THROMBOSIS LIMB ( 9 FDA reports)
VENTRICULAR DYSFUNCTION ( 9 FDA reports)
VIRAL LABYRINTHITIS ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ACCIDENT ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
ADRENAL NEOPLASM ( 8 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 8 FDA reports)
AORTIC VALVE SCLEROSIS ( 8 FDA reports)
AUTOIMMUNE DISORDER ( 8 FDA reports)
BACTERAEMIA ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 8 FDA reports)
BREAST INFECTION ( 8 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 8 FDA reports)
CERVICITIS ( 8 FDA reports)
CHAPPED LIPS ( 8 FDA reports)
COLD SWEAT ( 8 FDA reports)
COLITIS MICROSCOPIC ( 8 FDA reports)
CORONARY ARTERY OCCLUSION ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 8 FDA reports)
DEAFNESS TRAUMATIC ( 8 FDA reports)
DECREASED ACTIVITY ( 8 FDA reports)
DIFFICULTY IN WALKING ( 8 FDA reports)
EFFUSION ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
EPHELIDES ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
ERYTHEMA NODOSUM ( 8 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 8 FDA reports)
GINGIVAL ATROPHY ( 8 FDA reports)
GINGIVAL BLISTER ( 8 FDA reports)
GINGIVAL ERYTHEMA ( 8 FDA reports)
GINGIVAL HYPERPLASIA ( 8 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 8 FDA reports)
HIRSUTISM ( 8 FDA reports)
HORMONE LEVEL ABNORMAL ( 8 FDA reports)
HUNGER ( 8 FDA reports)
HYPERALBUMINAEMIA ( 8 FDA reports)
HYPERREFLEXIA ( 8 FDA reports)
HYPOTRICHOSIS ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
INCISION SITE PAIN ( 8 FDA reports)
INCREASED TENDENCY TO BRUISE ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
LENTIGO ( 8 FDA reports)
LHERMITTE'S SIGN ( 8 FDA reports)
LIP BLISTER ( 8 FDA reports)
LIP DRY ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
LYMPH GLAND INFECTION ( 8 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 8 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 8 FDA reports)
MAMMOGRAM ABNORMAL ( 8 FDA reports)
METASTASES TO PLEURA ( 8 FDA reports)
MUSCLE RUPTURE ( 8 FDA reports)
NASAL DISCOMFORT ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
OESOPHAGEAL STENOSIS ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
OSTEOCHONDROSIS ( 8 FDA reports)
OSTEOMYELITIS ACUTE ( 8 FDA reports)
OTITIS MEDIA ACUTE ( 8 FDA reports)
PAPILLOEDEMA ( 8 FDA reports)
PAPULE ( 8 FDA reports)
PARONYCHIA ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PHAEOCHROMOCYTOMA ( 8 FDA reports)
PLEURECTOMY ( 8 FDA reports)
PNEUMONIA BACTERIAL ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
QRS AXIS ABNORMAL ( 8 FDA reports)
RADIATION SKIN INJURY ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
RETINAL DEGENERATION ( 8 FDA reports)
RETINAL DISORDER ( 8 FDA reports)
RIB DEFORMITY ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SEXUAL DYSFUNCTION ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
SIGMOIDECTOMY ( 8 FDA reports)
SKIN INJURY ( 8 FDA reports)
SLUGGISHNESS ( 8 FDA reports)
SPINAL X-RAY ABNORMAL ( 8 FDA reports)
STERNAL FRACTURE ( 8 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 8 FDA reports)
TENDON SHEATH INCISION ( 8 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
TROPONIN INCREASED ( 8 FDA reports)
ULCER HAEMORRHAGE ( 8 FDA reports)
UVEITIS ( 8 FDA reports)
VAGINAL ODOUR ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ANURIA ( 7 FDA reports)
APICECTOMY ( 7 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
BLADDER CANCER RECURRENT ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLADDER PAIN ( 7 FDA reports)
BRAIN SCAN ABNORMAL ( 7 FDA reports)
BURSA DISORDER ( 7 FDA reports)
CARDIAC TAMPONADE ( 7 FDA reports)
CEREBRAL DISORDER ( 7 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
CYST REMOVAL ( 7 FDA reports)
CYSTOSCOPY ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DENTAL NECROSIS ( 7 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 7 FDA reports)
EAR CONGESTION ( 7 FDA reports)
EMBOLISM ( 7 FDA reports)
EPIGASTRIC DISCOMFORT ( 7 FDA reports)
FASCIITIS ( 7 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 7 FDA reports)
FORMICATION ( 7 FDA reports)
GALLBLADDER CANCER ( 7 FDA reports)
GASTROINTESTINAL TOXICITY ( 7 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 7 FDA reports)
HAIR COLOUR CHANGES ( 7 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
HYPERNATRAEMIA ( 7 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 7 FDA reports)
HYPERTENSIVE HEART DISEASE ( 7 FDA reports)
INJECTION SITE REACTION ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MEDIASTINAL DISORDER ( 7 FDA reports)
METABOLIC ALKALOSIS ( 7 FDA reports)
METASTASES TO NECK ( 7 FDA reports)
OCULAR VASCULAR DISORDER ( 7 FDA reports)
OPTIC ATROPHY ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PANCREATIC CARCINOMA ( 7 FDA reports)
PERICARDIAL DISEASE ( 7 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 7 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 7 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 7 FDA reports)
PUBIS FRACTURE ( 7 FDA reports)
RADIATION NEUROPATHY ( 7 FDA reports)
RADIATION OESOPHAGITIS ( 7 FDA reports)
RED BLOOD CELL ABNORMALITY ( 7 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 7 FDA reports)
REFLUX LARYNGITIS ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
SCAPULA FRACTURE ( 7 FDA reports)
SHOULDER OPERATION ( 7 FDA reports)
SINUS OPERATION ( 7 FDA reports)
SPINAL HAEMANGIOMA ( 7 FDA reports)
SPLINT APPLICATION ( 7 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 7 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 7 FDA reports)
TEARFULNESS ( 7 FDA reports)
THROMBOSIS IN DEVICE ( 7 FDA reports)
TRICHORRHEXIS ( 7 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 7 FDA reports)
UNDERDOSE ( 7 FDA reports)
VENOUS STENOSIS ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 7 FDA reports)
ACUTE LEUKAEMIA ( 6 FDA reports)
ADRENAL CARCINOMA ( 6 FDA reports)
ADVERSE REACTION ( 6 FDA reports)
ANAL PRURITUS ( 6 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
AORTIC VALVE REPAIR ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 6 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BONE CANCER METASTATIC ( 6 FDA reports)
BRAIN CANCER METASTATIC ( 6 FDA reports)
BREAST CANCER STAGE IV ( 6 FDA reports)
BREAST DISCOLOURATION ( 6 FDA reports)
BREAST FIBROSIS ( 6 FDA reports)
BRONCHIECTASIS ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CARDIAC OPERATION ( 6 FDA reports)
CAROTID ARTERY DISEASE ( 6 FDA reports)
CAUDA EQUINA SYNDROME ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CHOLECYSTITIS CHRONIC ( 6 FDA reports)
CLAVICLE FRACTURE ( 6 FDA reports)
COLLAPSE OF LUNG ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
COLOSTOMY ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 6 FDA reports)
CONTRALATERAL BREAST CANCER ( 6 FDA reports)
CORNEAL EROSION ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
DENTAL CLEANING ( 6 FDA reports)
DEPRESSION SUICIDAL ( 6 FDA reports)
DRUG LEVEL INCREASED ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
EAR DISCOMFORT ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
ENDOMETRIAL METAPLASIA ( 6 FDA reports)
ERYTHROMELALGIA ( 6 FDA reports)
FAILURE OF IMPLANT ( 6 FDA reports)
FEELING DRUNK ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FINGER DEFORMITY ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GASTROSTOMY TUBE INSERTION ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HOSPICE CARE ( 6 FDA reports)
INCISION SITE COMPLICATION ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
INJECTION SITE BRUISING ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 6 FDA reports)
INTESTINAL PERFORATION ( 6 FDA reports)
INTESTINAL ULCER ( 6 FDA reports)
ISCHAEMIC STROKE ( 6 FDA reports)
ISCHIORECTAL HERNIA ( 6 FDA reports)
JOINT DISLOCATION REDUCTION ( 6 FDA reports)
KETONURIA ( 6 FDA reports)
KIDNEY ENLARGEMENT ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
LYMPHOPENIA ( 6 FDA reports)
MALIGNANT ASCITES ( 6 FDA reports)
MALLORY-WEISS SYNDROME ( 6 FDA reports)
MANDIBULECTOMY ( 6 FDA reports)
METASTASES TO HEART ( 6 FDA reports)
METASTASES TO OVARY ( 6 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 6 FDA reports)
MONOCYTE COUNT INCREASED ( 6 FDA reports)
MONOPARESIS ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
MYASTHENIA GRAVIS ( 6 FDA reports)
NAIL DISCOLOURATION ( 6 FDA reports)
NASAL NEOPLASM ( 6 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 6 FDA reports)
NO THERAPEUTIC RESPONSE ( 6 FDA reports)
NONSPECIFIC REACTION ( 6 FDA reports)
ONYCHOGRYPHOSIS ( 6 FDA reports)
ONYCHOMADESIS ( 6 FDA reports)
ORTHOPEDIC PROCEDURE ( 6 FDA reports)
OTITIS EXTERNA ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 6 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PERIOSTITIS ( 6 FDA reports)
POLYMYALGIA RHEUMATICA ( 6 FDA reports)
POSTOPERATIVE ADHESION ( 6 FDA reports)
PRESBYOPIA ( 6 FDA reports)
PROTHROMBIN TIME SHORTENED ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
RECTAL POLYP ( 6 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 6 FDA reports)
SCINTIGRAPHY ( 6 FDA reports)
SENSATION OF FOREIGN BODY ( 6 FDA reports)
SKIN FIBROSIS ( 6 FDA reports)
SKIN GRAFT ( 6 FDA reports)
SKIN ODOUR ABNORMAL ( 6 FDA reports)
SKIN PLAQUE ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SOFT TISSUE MASS ( 6 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 6 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 6 FDA reports)
SUBCUTANEOUS NODULE ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
TRANSFERRIN DECREASED ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
URINARY TRACT DISORDER ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
UTERINE FIBROSIS ( 6 FDA reports)
VESTIBULITIS ( 6 FDA reports)
VITAMIN E DEFICIENCY ( 6 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 6 FDA reports)
WISDOM TEETH REMOVAL ( 6 FDA reports)
ABDOMINAL INFECTION ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
ANAL SPHINCTER ATONY ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
AURICULAR PERICHONDRITIS ( 5 FDA reports)
AUTOIMMUNE THYROIDITIS ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD MAGNESIUM INCREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 5 FDA reports)
BONE DENSITY ABNORMAL ( 5 FDA reports)
BRADYKINESIA ( 5 FDA reports)
BRAIN OPERATION ( 5 FDA reports)
BREAST CELLULITIS ( 5 FDA reports)
BREAST ENLARGEMENT ( 5 FDA reports)
BREAST NECROSIS ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
BRONCHITIS VIRAL ( 5 FDA reports)
CALCULUS BLADDER ( 5 FDA reports)
CALCULUS URETERIC ( 5 FDA reports)
CANCER IN REMISSION ( 5 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 5 FDA reports)
CEREBELLAR ATROPHY ( 5 FDA reports)
CEREBRAL THROMBOSIS ( 5 FDA reports)
CHOKING ( 5 FDA reports)
CHONDROPLASTY ( 5 FDA reports)
CHYLOTHORAX ( 5 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 5 FDA reports)
COELIAC DISEASE ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CORNEAL OEDEMA ( 5 FDA reports)
DEAFNESS BILATERAL ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIABETIC RETINOPATHY ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DYSAESTHESIA ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ENDOMETRIAL SARCOMA ( 5 FDA reports)
FOOD CRAVING ( 5 FDA reports)
FRACTURE REDUCTION ( 5 FDA reports)
GALLBLADDER OPERATION ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTRIC OPERATION ( 5 FDA reports)
GLIOSIS ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HYDROURETER ( 5 FDA reports)
HYPERAMMONAEMIA ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
IMPACTED FRACTURE ( 5 FDA reports)
IMPETIGO ( 5 FDA reports)
INFARCTION ( 5 FDA reports)
INJECTION SITE DISCOMFORT ( 5 FDA reports)
IRIS ADHESIONS ( 5 FDA reports)
KNEE DEFORMITY ( 5 FDA reports)
KYPHOSCOLIOSIS ( 5 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LIMB OPERATION ( 5 FDA reports)
LUNG CANCER METASTATIC ( 5 FDA reports)
LYMPHANGITIS ( 5 FDA reports)
MEDICAL DEVICE COMPLICATION ( 5 FDA reports)
METASTASES TO PELVIS ( 5 FDA reports)
METASTATIC LYMPHOMA ( 5 FDA reports)
MUCOSAL NECROSIS ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NASAL DISORDER ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 5 FDA reports)
OESOPHAGEAL SPASM ( 5 FDA reports)
OMENTUM NEOPLASM ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
ORBITAL OEDEMA ( 5 FDA reports)
OROPHARYNGEAL PLAQUE ( 5 FDA reports)
OVARIAN ENLARGEMENT ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PELVIC NEOPLASM ( 5 FDA reports)
POST PROCEDURAL FISTULA ( 5 FDA reports)
POST PROCEDURAL HAEMATOMA ( 5 FDA reports)
POSTNASAL DRIP ( 5 FDA reports)
POSTOPERATIVE ABSCESS ( 5 FDA reports)
PREMATURE AGEING ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
PULMONARY HILUM MASS ( 5 FDA reports)
PYOGENIC GRANULOMA ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 5 FDA reports)
RETINAL MELANOMA ( 5 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 5 FDA reports)
SIALOADENITIS ( 5 FDA reports)
TENSION ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
THORACIC OUTLET SYNDROME ( 5 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
THROMBOCYTOSIS ( 5 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
TOOTH DECALCIFICATION ( 5 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
URINE OUTPUT INCREASED ( 5 FDA reports)
UTERINE ENLARGEMENT ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
VAGINITIS BACTERIAL ( 5 FDA reports)
VITAMIN B12 INCREASED ( 5 FDA reports)
VITAMIN D ABNORMAL ( 5 FDA reports)
VULVAL ABSCESS ( 5 FDA reports)
WOUND NECROSIS ( 5 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ADHESION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ALKALOSIS ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAL CANCER ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANHIDROSIS ( 4 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
APLASIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIAL STENOSIS LIMB ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 4 FDA reports)
BLOOD COUNT ABNORMAL ( 4 FDA reports)
BLOOD DISORDER ( 4 FDA reports)
BLOOD IRON INCREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BONE DECALCIFICATION ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE OEDEMA ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRADYPHRENIA ( 4 FDA reports)
BREAST CANCER STAGE I ( 4 FDA reports)
BREAST DISORDER FEMALE ( 4 FDA reports)
BREAST NEOPLASM ( 4 FDA reports)
BUNION OPERATION ( 4 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CATHETER SITE RELATED REACTION ( 4 FDA reports)
CATHETERISATION VENOUS ( 4 FDA reports)
CELLULITIS ORBITAL ( 4 FDA reports)
CEREBELLAR INFARCTION ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
CHONDROPATHY ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COLON CANCER STAGE III ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
COR PULMONALE CHRONIC ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DIPLEGIA ( 4 FDA reports)
DROOLING ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DUPUYTREN'S CONTRACTURE ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
EAR CANAL ERYTHEMA ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
ENDOMETRIAL NEOPLASM ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
EPIPHYSIOLYSIS ( 4 FDA reports)
ETHMOID SINUS SURGERY ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
EXERCISE TEST ABNORMAL ( 4 FDA reports)
EXPLORATIVE LAPAROTOMY ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
FAT NECROSIS ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FRACTURE TREATMENT ( 4 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GENITAL DISORDER FEMALE ( 4 FDA reports)
GINGIVAL DISCOLOURATION ( 4 FDA reports)
GINGIVAL OPERATION ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HEPATIC VEIN THROMBOSIS ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERVITAMINOSIS ( 4 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INSULINOMA ( 4 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JOINT CONTRACTURE ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LIVER ABSCESS ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
MASTOID DISORDER ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 4 FDA reports)
OVARIAN ATROPHY ( 4 FDA reports)
OVARIAN DISORDER ( 4 FDA reports)
PACEMAKER COMPLICATION ( 4 FDA reports)
PANCREATIC ENZYMES INCREASED ( 4 FDA reports)
PARACENTESIS ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 4 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PNEUMONITIS CHEMICAL ( 4 FDA reports)
POLYP COLORECTAL ( 4 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 4 FDA reports)
POSTOPERATIVE INFECTION ( 4 FDA reports)
PRODUCT TASTE ABNORMAL ( 4 FDA reports)
PSEUDARTHROSIS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PULMONARY CALCIFICATION ( 4 FDA reports)
RADIATION PNEUMONITIS ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
RECTOCELE REPAIR ( 4 FDA reports)
REHABILITATION THERAPY ( 4 FDA reports)
RETINAL ARTERY THROMBOSIS ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SINUS ANTROSTOMY ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 4 FDA reports)
SPINAL PAIN ( 4 FDA reports)
SPONDYLOLYSIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 4 FDA reports)
SYNCOPE VASOVAGAL ( 4 FDA reports)
TESTICULAR MICROLITHIASIS ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THORACOTOMY ( 4 FDA reports)
TOE OPERATION ( 4 FDA reports)
TRACHEAL PAIN ( 4 FDA reports)
TRANSFUSION REACTION ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
TUMOUR MARKER TEST ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
UROGRAM ( 4 FDA reports)
UTERINE DILATION AND CURETTAGE ( 4 FDA reports)
VAGINAL INFLAMMATION ( 4 FDA reports)
VASCULAR FRAGILITY ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VIIITH NERVE LESION ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
WEIGHT FLUCTUATION ( 4 FDA reports)
X-RAY DENTAL ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS SOFT TISSUE ( 3 FDA reports)
ACARODERMATITIS ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADENOTONSILLECTOMY ( 3 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
APATHY ( 3 FDA reports)
APPARENT DEATH ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
ARTERIAL DISORDER ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
ARTICULAR CALCIFICATION ( 3 FDA reports)
ASPIRATION BREAST ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BIOPSY SKIN ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BONE NEOPLASM ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREAST CANCER STAGE III ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 3 FDA reports)
CARDIAC ANEURYSM ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHRONIC FATIGUE SYNDROME ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CRANIECTOMY ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CUTIS LAXA ( 3 FDA reports)
CYCLOTHYMIC DISORDER ( 3 FDA reports)
CYTOREDUCTIVE SURGERY ( 3 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DISLOCATION OF VERTEBRA ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG INTERACTION POTENTIATION ( 3 FDA reports)
DRY SOCKET ( 3 FDA reports)
EAR PRURITUS ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 3 FDA reports)
EXTENSIVE INTERDIALYTIC WEIGHT GAIN ( 3 FDA reports)
EXTRASKELETAL OSSIFICATION ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
FACIAL LESION EXCISION ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FRACTURE DELAYED UNION ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GASTRIC INFECTION ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROSTOMY FAILURE ( 3 FDA reports)
GENERAL ANAESTHESIA ( 3 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HYPEROXIA ( 3 FDA reports)
HYPERSPLENISM ( 3 FDA reports)
HYPOGONADISM ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
INADEQUATE ANALGESIA ( 3 FDA reports)
INFECTED CYST ( 3 FDA reports)
INGROWN HAIR ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
JOINT DESTRUCTION ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LAPAROSCOPY ABNORMAL ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
LIBIDO INCREASED ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LUNG INJURY ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MARITAL PROBLEM ( 3 FDA reports)
MASTOIDECTOMY ( 3 FDA reports)
MEDICATION RESIDUE ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 3 FDA reports)
MICTURITION DISORDER ( 3 FDA reports)
MIXED HYPERLIPIDAEMIA ( 3 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 3 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NAIL GROWTH ABNORMAL ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESTRADIOL DECREASED ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL BLISTERING ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OVERWEIGHT ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PALPABLE PURPURA ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PERSISTENT GENERALISED LYMPHADENOPATHY ( 3 FDA reports)
PHIMOSIS ( 3 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POST LAMINECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL SWELLING ( 3 FDA reports)
PREMENSTRUAL SYNDROME ( 3 FDA reports)
PROCEDURAL HYPERTENSION ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PSYCHOSOMATIC DISEASE ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
PYELOGRAM RETROGRADE ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADIATION NECROSIS ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SALIVA DISCOLOURATION ( 3 FDA reports)
SCAB ( 3 FDA reports)
SECONDARY SEQUESTRUM ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOULDER ARTHROPLASTY ( 3 FDA reports)
SINUS ARRHYTHMIA ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SOPOR ( 3 FDA reports)
SPINAL COLUMN INJURY ( 3 FDA reports)
SPINAL CORD INFARCTION ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
TESTICULAR HYPERTROPHY ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THYROID PAIN ( 3 FDA reports)
TOE DEFORMITY ( 3 FDA reports)
TOXIC SHOCK SYNDROME ( 3 FDA reports)
URETHRAL DISORDER ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URETHRAL OBSTRUCTION ( 3 FDA reports)
URETHRAL STENT INSERTION ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VARICOSE VEIN RUPTURED ( 3 FDA reports)
VASCULAR PURPURA ( 3 FDA reports)
VEIN DISCOLOURATION ( 3 FDA reports)
VISUAL BRIGHTNESS ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VOMITING PROJECTILE ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACNE CYSTIC ( 2 FDA reports)
ACROMEGALY ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANDROGENETIC ALOPECIA ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AUTOMATIC BLADDER ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BENIGN OVARIAN TUMOUR ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY ENDOMETRIUM ( 2 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CALCIUM ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM ABNORMAL ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST HAEMORRHAGE ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERVIX ENLARGEMENT ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORRECTIVE LENS USER ( 2 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CUBITAL TUNNEL SYNDROME ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DEHYDROEPIANDROSTERONE TEST ( 2 FDA reports)
DEJA VU ( 2 FDA reports)
DEMENTIA WITH LEWY BODIES ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG NAME CONFUSION ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ECTROPION OF CERVIX ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ENAMEL ANOMALY ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERALDOSTERONISM ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
IMMUNISATION ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
IODINE UPTAKE INCREASED ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT STABILISATION ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 2 FDA reports)
LARYNGEAL CYST ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG WEDGE RESECTION ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MELAS SYNDROME ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
METASTASES TO ABDOMINAL WALL ( 2 FDA reports)
METASTASES TO BREAST ( 2 FDA reports)
METASTASES TO GALLBLADDER ( 2 FDA reports)
METASTASES TO RETROPERITONEUM ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYASTHENIC SYNDROME ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NAIL INJURY ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESTRADIOL ABNORMAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORAL PUSTULE ( 2 FDA reports)
OSTEOTOMY ( 2 FDA reports)
OVARIAN ADENOMA ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OVULATION DISORDER ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 2 FDA reports)
PARACENTESIS ABDOMEN ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PELIOSIS HEPATIS ( 2 FDA reports)
PERINEURIAL CYST ( 2 FDA reports)
PERIODONTAL DESTRUCTION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARYNGEAL NEOPLASM ( 2 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCOLLAGEN TYPE I C-TERMINAL PROPEPTIDE INCREASED ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RECTAL OBSTRUCTION ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL GLYCOSURIA ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOSCHISIS ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEBACEOUS GLANDS OVERACTIVITY ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPINOCEREBELLAR ATAXIA ( 2 FDA reports)
SPLEEN SCAN ABNORMAL ( 2 FDA reports)
SPLENIC HAEMATOMA ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SUPERINFECTION BACTERIAL ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TARSAL TUNNEL SYNDROME ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THYROID FUNCTION TEST NORMAL ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC ARTHRITIS ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TUMOUR EMBOLISM ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TUMOUR ULCERATION ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY HESITATION ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE CERVIX ATROPHY ( 2 FDA reports)
VAGINAL NEOPLASM ( 2 FDA reports)
VAGINAL POLYP ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVAR DYSPLASIA ( 2 FDA reports)
VULVOVAGINITIS ( 2 FDA reports)
WRIST SURGERY ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL HYSTERECTOMY ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 1 FDA reports)
AFFERENT LOOP SYNDROME ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALOPECIA SCARRING ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SKIN TAG EXCISION ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASTEATOSIS ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AURA ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BENIGN NEOPLASM OF EYE ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILEVEL POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY CERVIX ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRACHYTHERAPY ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CYST DRAINAGE ( 1 FDA reports)
BREAST HAEMATOMA ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST SARCOMA ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
CALCIUM DEFICIENCY ( 1 FDA reports)
CALLUS FORMATION DELAYED ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARTILAGE ATROPHY ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL DISCHARGE ( 1 FDA reports)
CERVIX CARCINOMA STAGE II ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHLOASMA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLUMSY CHILD SYNDROME ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC ATONY ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLORECTAL CANCER STAGE III ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 1 FDA reports)
DELAYED CLOSURE OF CRANIAL SUTURES ( 1 FDA reports)
DENTAL DISORDER PROPHYLAXIS ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DISORDER OF SEX DEVELOPMENT ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTROPION ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
ERYTHEMA MIGRANS ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE IRRIGATION ( 1 FDA reports)
EYELASH THICKENING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEAR OF CROWDED PLACES ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE SEX HORMONE LEVEL ABNORMAL ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL CYST ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GRIP STRENGTH ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEAT OEDEMA ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC EMBOLISATION ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ADENOCARCINOMA ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LAPAROSCOPY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOW TENSION GLAUCOMA ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUMBOSACRAL PLEXUS INJURY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT NEOPLASM OF UTERINE ADNEXA ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MAMMOGRAM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MAXIMAL VOLUNTARY VENTILATION ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIAN NERVE INJURY ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO TRACHEA ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL DISCOMFORT ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OESOPHAGEAL CARCINOMA RECURRENT ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY NEGATIVE ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL FIBROMA ( 1 FDA reports)
ORAL NEOPLASM BENIGN ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
PAGET'S DISEASE OF THE VULVA ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATICOSPLENECTOMY ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PAROPHTHALMIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHLEBITIS ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PITYRIASIS RUBRA PILARIS ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POVERTY ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT CONTAMINATION CHEMICAL ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROMOTION OF WOUND HEALING ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYOMETRA ( 1 FDA reports)
RADICULAR CYST ( 1 FDA reports)
RADIOTHERAPY TO BREAST ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ANOMALY CONGENITAL ( 1 FDA reports)
RETINAL CYST ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINOTRACHEITIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEROLOGY ABNORMAL ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHOPLIFTING ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SLOW VIRUS INFECTION ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOMA SITE REACTION ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUCROSE INTOLERANCE ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROGLOBULIN INCREASED ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TINEA MANUUM ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH AVULSION ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETHRAL CARUNCLE ( 1 FDA reports)
URETHRAL SPASM ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE INVERSION ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE POLYPECTOMY ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL STRICTURE ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR SKIN DISORDER ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VATER SYNDROME ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL SINUSITIS ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY ABNORMAL ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITREOUS ADHESIONS ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL DISORDER ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)

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