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

DYSPNOEA ( 12 FDA reports)
FALL ( 11 FDA reports)
PAIN ( 11 FDA reports)
DEPRESSION ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
NAUSEA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
CHILLS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
ILEUS ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTROINTESTINAL STENOSIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MONOCLONAL GAMMOPATHY ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NERVE INJURY ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
THROMBOCYTHAEMIA ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FISTULA ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INTESTINAL RESECTION ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
LISTERIOSIS ( 3 FDA reports)
LUPUS-LIKE SYNDROME ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CEREBRAL HAEMANGIOMA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROSTOMY ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPLANT SITE INFLAMMATION ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACNE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIPOSARCOMA METASTATIC ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MANIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARASITIC INFECTION INTESTINAL ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PERINEAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VITAMIN B6 DEFICIENCY ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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